Char syndrome

Char syndrome is an autosomal dominant trait characterized by patent ductus arteriosus, facial dysmorphism and hand anomalies. Using a positional candidacy strategy, we mapped TFAP2B, encoding a transcription factor expressed in neural crest cells, to the Char syndrome critical region and identified … The Charcot-Marie-Tooth (CMT) Support Community connects patients, families, friends and caregivers for support and inspiration. This community is sponsored by the Hereditary Neuropathy Foundation, an Inspire trusted partner.Axenfeld-Rieger syndrome (ARS) is a rare genetic disorder that affects the eye as well as other parts of the body. It is estimated to occur in approximately 1 person in 50,000 worldwide. The disorder affects males and females equally and has been observed in patients from various ethnic backgrounds from all over the world.翻译 API; 关于 MyMemory; 登录 ...Jan 19, 2022 · Char syndrome is a rare genetic condition that affects how a baby’s face, heart, and hands develop. It’s been found in only a few families worldwide. People with the condition have distinctive... CHARGE syndrome is associated with characteristic external ears that tend to protrude and lack lobes. The hearing loss can range from a mild hearing loss to profound deafness. Hearing loss can be very difficult to measure in young children. Many children with CHARGE receive cochlear implants to aid their sensorineural hearing loss.Charcot-Wilbrand syndrome is considered a rare condition since it has very little incidence among the population. Although this implies a lack of studies investigating it, it has been recognized as a condition related to focal brain damage. Its possible negative effects,Charcot affects the bones, joints, and soft tissues of the foot or ankle. The bones become weak and can break and the joints in the foot or ankle can dislocate. If not caught in its earliest stage, the joints in the foot collapse and the foot eventually becomes deformed. A deformed foot can cause pressure sores to develop in the foot or ankle.Aug 15, 2003 · Char syndrome is inherited in an autosomal dominant manner. The proportion of cases caused by a de novo pathogenic variant is unknown. If a parent of the proband is affected, the risk to the sibs is 50%. When the parents are clinically unaffected, the risk to the sibs of a proband appears to be low. Axenfeld-Rieger syndrome (ARS) is a rare genetic disorder that affects the eye as well as other parts of the body. It is estimated to occur in approximately 1 person in 50,000 worldwide. The disorder affects males and females equally and has been observed in patients from various ethnic backgrounds from all over the world. ethernet cable splitter Crouzon syndrome, also known as craniofacial dysotosis, is a genetic syndrome in which the seams of the skull fuse in abnormally. This affects the shape of the head and face. It is the most common type of syndromic craniosynostosis. Gene mutations are responsible for the abnormal skull fusions. Crouzon syndrome shares many of the same features ...The disorder is characterized by intellectual disability and delayed development, small head size ( microcephaly ), low birth weight, and weak muscle tone (hypotonia) in infancy. Affected individuals also have distinctive facial features, including widely set eyes (hypertelorism), low-set ears, a small jaw, and a rounded face.翻译 API; 关于 MyMemory; 登录 ...Synonyms of char (Entry 1 of 2) a female domestic servant a busy executive who leaves most of the cooking and cleaning to the char Synonyms for char biddy, charwoman, handmaiden (also handmaid), house girl, housekeeper, housemaid, maid, maidservant, skivvy [ British ], wench char verb Synonyms of char (Entry 2 of 2) to burn on the surfacewho won the battle of fort sumter north or south. hyundai santa fe check urea system. overlord x male reader wattpad; sklearn linear regression positive coefficients Summary. Mosaic Down syndrome is a rare form of Down syndrome — a genetic condition that causes an extra chromosome to appear in a person's DNA. Human DNA typically contains 23 pairs of ...The disorder mapping to chromosome 17 was referred to as Charcot-Marie-Tooth disease type 1A or hereditary motor and sensory neuropathy type I (HMSN I). In studies of 7 families, Chance et al. ( 1989, 1990) found a high probability of linkage to chromosome 17 markers in 5.Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger Anadolu Kardiyol Derg . 2012 Sep;12(6):523-4. doi: 10.5152/akd.2012.165. Citisli V. Assessment of diagnosis and treatment of thoracic outlet syndrome , an important reason of pain in upper extremity, based on literature. J Pain Relief ... Nov 27, 2000 · This report describes a father and daughter with Char syndrome, a rare autosomal dominant disorder. Both affected individuals had typical face, strabismus, and foot anomalies. The girl also had a patent ductus arteriosus. In addition, both patients had polythelia (supernumerary nipples), a finding not described before in the Char syndrome. a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by the triad of patent ductus arteriosus (pda), facial dysmorphism (wide-set eyes, downslanting palpebral fissures, mild ptosis, flat midface, flat nasal bridge and upturned nasal tip, short philtrum with a triangular mouth, and thickened, everted lips) and hand … Nov 27, 2000 · This report describes a father and daughter with Char syndrome, a rare autosomal dominant disorder. Both affected individuals had typical face, strabismus, and foot anomalies. The girl also had a patent ductus arteriosus. In addition, both patients had polythelia (supernumerary nipples), a finding not described before in the Char syndrome. Charcot-Marie-Tooth disease is a large group of clinically and genetically heterogeneous disorders characterized by progressive motor and sensory polyneuropathy. These can be separated (with overlap) into two large groups on the basis of electrophysiologic criteria: type 1 is the demyelinating form, and type 2 the axonal form.Charcot-Marie Tooth Syndrome Definition and Causes - the Charcot-Marie-Tooth Syndrome or CMT is an inherited peripheral polyneuropathy first described independently by French professor Jean-Martin Charcot and his student Pierre Marie in 1886 and later by Howard Henry Tooth in his dissertation in the same year (PatientPlus 2005, Kedlaya 2005).If you are an student, you may probably will have to solve the problematic of printing a square with some character, usually an asterisk, of X length in some predefined programming language. Char syndrome. Fifth middle phalanges are absent, and fifth proximal and distal phalanges are hypoplastic. Figure 3. Genetic map locations of linked markers on chromo-some 6 defining the Char syndrome locus. Recombination dis-tances in centimorgans (cM) are shown as determined by Mu¨cher and coworkers.14 Bar at right indicates most likelyChar syndrome is an autosomal dominant disorder comprising facial dysmorphism, hand anomalies, and patent ductus arteriosus (PDA). In this report, we describe a proband with a de novo TFAP2B frameshift mutation c.650delG p. (Gly217Alafs*32) in the basic domain. The proband presented mainly with musculoskeletal features of Char syndrome. crypt tv Char syndrome is inherited in an autosomal dominant manner. The proportion of cases caused by a de novo pathogenic variant is unknown. If a parent of the proband is affected, the risk to the sibs is 50%. When the parents are clinically unaffected, the risk to the sibs of a proband appears to be low.Member types char_type, traits_type and allocator_type are the class template parameters of basic_stringstream. Return Value For (1), a basic_string object with a copy of the current contents in the stream buffer. Member types char_type, traits_type and allocator_type are the class template parameters of basic_stringstream. Example. Charcot-Marie-Tooth disease is an autosomal dominant condition characterised by slowly progressive sensorimotor neuropathy. It is the most commonly inherited peripheral neuropathy in the UK. Lifespan is normal. Disability is usually mild. Last reviewed 01/2018 Links: genetics clinical featuresA diagnosis of Charcot syndrome should be considered in any neuropathic patient, even those with a minor increase of heat and swelling of the foot or ankle, especially after any injury. Early ...The Charcot-Marie-Tooth (CMT) Support Community connects patients, families, friends and caregivers for support and inspiration. This community is sponsored by the Hereditary Neuropathy Foundation, an Inspire trusted partner.Oct 19, 2012 - Charcot-Marie-Tooth Disease, a disease that causes degeneration of the nerves which leads to muscle deterioration. It begins in the arms and legs, but eventually effects the whole body . See more ideas about teeth diseases, disease, cmt.Workplace Enterprise Fintech China Policy Newsletters Braintrust lowest presidential approval ratings Events Careers springdale utah real estate Member types char_type, traits_type and allocator_type are the class template parameters of basic_stringstream. Return Value For (1), a basic_string object with a copy of the current contents in the stream buffer. Member types char_type, traits_type and allocator_type are the class template parameters of basic_stringstream. Example. shower tower Charcot-Marie-Tooth disease (CMT), also called hereditary motor and sensory neuropathy (HMSN), is a group of inherited neurological disorders affecting an estimated 2.8 million adults and children worldwide. Gene mutations reduce the ability of peripheral nerves to carry motor and sensory information, typically resulting in pain and slowly ...Charcot-Marie-Tooth disease type 2 (CMT2) is a type of CMT whose genetic defects, or mutations, disrupt the structure and function of axons — the long projections of nerve cells that conduct signals to the next nerve cell or muscle cell. ... CMT2 sometimes is associated with a treatable condition called restless leg syndrome, an irresistible ...Jan 17, 2020 - Explore Anita Jordan's board "CMT Charcot Marie Tooth", followed by 112 people on Pinterest. See more ideas about cmt, teeth diseases, fibromyalgia.who won the battle of fort sumter north or south. hyundai santa fe check urea system. overlord x male reader wattpad; sklearn linear regression positive coefficients Char syndrome is a rare genetic condition that affects how a baby's face, heart, and hands develop. It's been found in only a few families worldwide. People with the condition have distinctive...Cri du chat syndrome is a rare genetic disorder caused by a missing section on a particular chromosome known as Chromosome 5. Sometimes, material from another chromosome is missing as well. Around one in every 50,000 or so babies is diagnosed with this disorder. This estimate is coming down.The meaning of CHARCOT-MARIE-TOOTH DISEASE is an inherited neurological disorder affecting the peripheral nerves that is marked especially by progressive muscular weakness in the foot and lower leg and later the forearms and hands and that typically has an onset during adolescence or early adulthood —called also peroneal muscular atrophy.Aug 15, 2003 · Char syndrome is characterized by the triad of typical facial features, patent ductus arteriosus, and aplasia or hypoplasia of the middle phalanges of the fifth fingers. Typical facial features are depressed nasal bridge and broad flat nasal tip, widely spaced eyes, downslanted palpebral fissures, mild ptosis, short philtrum with prominent philtral ridges with an upward pointing vermilion border resulting in a triangular mouth, and thickened (patulous) everted lips. Share this entry. Anyone you share the following link with will be able to read this content: Get shareable linkOral allergy syndrome can cause cross-reactions in people allergic to things like grass pollen and latex. It can cause itchiness from raw produce. bcbgmaxazria dresses Charcot foot is a serious complication which can affect persons with peripheral neuropathy, especially those with diabetes mellitus. This is a condition in which the nerves in the lower legs and feet have been damaged. The damage causes a loss of sensation in the feet. It affects the bones, joints, and soft tissues of the foot and ankle. [1]I have joined this forum totally to support you and raise awareness for chair sliding syndrome. I have pretty much exact same symptoms, unconscious sliding till my chest is at 45' or my thighs are horizontal. Realising at this point I have horrendous posture, I re-seat my arse and straighten up everything - feet, legs, hips, back, shoulders ...char·cu·ter·ie (shär-ko͞o′tə-rē′, -ko͞o′tə-rē) n. 1. Sausages, ham, pâtés, and other cooked or processed meat foods. 2. A delicatessen specializing in such foods. [French, from chaircuicterie : chair, meat (from Latin carō, flesh; see carnage) + cuict, cuit, cooked (from Latin coctus, past participle of coquere; see cook).] American ...The diabetic Charcot foot syndrome is a serious and potentially limb-threatening lower-extremity complication of diabetes. First described in 1883, this enigmatic condition continues to challenge even the most experienced practitioners.This disease was referred to as Hoffman disease and later was known as Charcot-Marie-Tooth-Hoffman disease. In 1968, CMT disease was subdivided into two types, CMT 1 and CMT 2, on the basis of...Char syndrome is a condition that affects the development of the face, heart, and limbs. It is characterized by a combination of three major features: a distinctive facial appearance, a heart defect called patent ductus arteriosus, and hand abnormalities.People living with Char syndrome have distinguishing facial features, a heart abnormality known as patent ductus arteriosus, and hand anomalies. Someone with Char syndrome might have a flatter than normal nose tip and nasal bridge, as well as flatter cheekbones. The eyes will be set apart and turn downwards, giving the person a "droopy ...Oct 19, 2012 - Charcot-Marie-Tooth Disease, a disease that causes degeneration of the nerves which leads to muscle deterioration. It begins in the arms and legs, but eventually effects the whole body . See more ideas about teeth diseases, disease, cmt.Roussy- Lévy Syndrome is used to describe a phenotype (or expression of symptoms) that includes high arches, loss of reflexes, distal limb weakness, tremor in the upper limbs, distal sensory loss and gait ataxia (lack of coordination), probably due to the sensory symptoms. This can also be associated with a form of scoliosis called kyphosis.Chargriller.com is a Food and Drink website created by Char-Griller.This domain provided by cscdbs.com at 1998-08-11T04:00:00Z (23 Years, 279 Days ago), expired at 2026-08. starter dreadsharley quinn tv seriesCrouzon syndrome, also known as craniofacial dysotosis, is a genetic syndrome in which the seams of the skull fuse in abnormally. This affects the shape of the head and face. It is the most common type of syndromic craniosynostosis. Gene mutations are responsible for the abnormal skull fusions. Crouzon syndrome shares many of the same features ...Charcot-Marie-Tooth disease may sometimes cause pain due to muscle cramps or nerve damage. If pain is an issue for you, prescription pain medication may help control your pain. Therapy. Physical therapy. Physical therapy can help strengthen and stretch your muscles to prevent muscle tightening and loss. A program usually includes low-impact ...Char syndrome is a condition that affects the development of the face, heart, and limbs. It is characterized by a combination of three major features: a distinctive facial appearance, a heart defect called patent ductus arteriosus, and hand abnormalities.Charcot-Marie-Tooth disease is a group of disorders that affect the peripheral nerves, the nerves running from outside the brain and spine. Note: There are currently no drugs listed for "Charcot-Marie-Tooth Disease". Learn more about Charcot-Marie-Tooth Disease Mayo Clinic reference Charcot-Marie-Tooth disease Browse treatment options A B C D E F GChar syndrome. Heart-hand syndrome characterized by unusual facial features including long philtrum, down-slanting palpebral fissures, thick lips as well as patent ductus arteriosus and abnormal fifth digits. From mutation in TFAP2B. Charcot-Bouchard aneurysmsChar syndrome is a condition that affects the development of the face, heart, and limbs. It is characterized by a combination of three major features: a distinctive facial appearance, a heart defect called patent ductus arteriosus, and hand abnormalities. After the time is up in the freezer, grease a cooking rack and transfer the loaf out of the pan and onto the rack. With the Char-Griller Gravity 980 running at 350 degrees and some hickory smoke going, place the rack in the center of the grate until the center of the meatloaf reaches 165 degrees (roughly an hour). who won the battle of fort sumter north or south. hyundai santa fe check urea system. overlord x male reader wattpad; sklearn linear regression positive coefficients Charcot foot, also known as Neurogenic Osteoarthropathy is an extremely complicated and potentially catastrophic condition effecting the foot, ankle and lower leg, which may result in amputation it not treated swiftly. In order for a patient to develop Charcot Foot, they must first have foot neuropathy.A character type. The char type represents a single character. More specifically, since 'character' isn't a well-defined concept in Unicode, char is a 'Unicode scalar value', which is similar to, but not the same as, a 'Unicode code point'. This documentation describes a number of methods and trait implementations on the char type. For ... Summary. Is a 153 gene panel that includes assessment of non-coding variants. Is ideal for patients with a clinical suspicion of Charcot-Marie-Tooth neuropathy. * The CPT codes provided are based on AMA guidelines and are for informational purposes only. see through underwear 翻译 API; 关于 MyMemory; 登录 ...Charles Bonnet Syndrome. (pronounced bo NAY) is a condition that causes people with decreased vision and various eye diseases to have visual hallucinations. These hallucinations can include seeing patterns, or more complex images such as people, animals, flowers, and buildings. CBS is named after the 18th century Swiss scientist, Charles Bonnet ...Char syndrome is a condition that affects the development of the face, heart, and limbs. It is characterized by a combination of three major features: a distinctive facial appearance, a heart defect called patent ductus arteriosus, and hand abnormalities.Roast tenderloins on center rack of 350° oven for 20 minutes. Remove from oven and reprogram oven to broil, with oven rack positioned 5 1/2"-6" under heat. Using a pastry brush, paint a light coating of glaze on the surface of both tenderloins. Place under broiler for 3 minutes.In the United States, this deformity most commonly occurs in people with diabetes. The foot first enters an acute stage of swelling, warmth, and redness that can be mistaken for an infection. Broken bones and dislocations can occur, causing severe deformities of the foot and ankle.Partly because there are different types of Charcot-Marie-Tooth disease (CMT), the exact symptoms vary greatly from person to person. This section presents a general picture of CMT signs and symptoms. Contractures and bone deformities The most common initial presentation of CMT is distal weakness and atrophy, which manifest with foot drop and pes cavus (high arched feet).Char syndrome is inherited in an autosomal dominant manner. The proportion of cases caused by a de novo pathogenic variant is unknown. If a parent of the proband is affected, the risk to the sibs is 50%. When the parents are clinically unaffected, the risk to the sibs of a proband appears to be low.Objective: To describe the diagnostic yield and prognosis for patients with hemisensory syndrome. Background: The aetiology, utility of diagnostic procedures, and outcome of hemisensory syndrome in patients with exclusive hemibody complaints having only subjective sensory abnormalities on examination is unknown. Methods: Patients were prospectively identified with hemisensory syndrome in a ... point ruston People living with Char syndrome have distinguishing facial features, a heart abnormality known as patent ductus arteriosus, and hand anomalies. Someone with Char syndrome might have a flatter than normal nose tip and nasal bridge, as well as flatter cheekbones. The eyes will be set apart and turn downwards, giving the person a "droopy ...A diagnosis of Charcot syndrome should be considered in any neuropathic patient, even those with a minor increase of heat and swelling of the foot or ankle, especially after any injury. Early ...its when some kids you know suddenly tries to act cool like they are the main character of a show.but mostly its just childish delusions for example like when you see someone trying to act like a anime character then you know he or she has eighth grade syndrome.charcot marie tooth syndrome - MedHelp's charcot marie tooth syndrome Center for Information, Symptoms, Resources, Treatments and Tools for charcot marie tooth syndrome. Find charcot marie tooth syndrome information, treatments for charcot marie tooth syndrome and charcot marie tooth syndrome symptoms.Summary. Charcot-Marie-Tooth disease (CMT) is the umbrella term for a range of inherited genetic conditions affecting the peripheral nervous system (the nerves stretching from the spinal cord to the muscles). Symptoms include progressive weakness and muscle wasting of the legs and arms. The ways people are affected can vary widely.The North Carolina Down Syndrome Alliance is committed to helping our staff and their families, our community groups, partners, and the Down syndrome community to stay healthy by doing what we can to prevent the spread of the coronavirus, COVID-19. To help mitigate the impact of this evolving public health issue, NCDSA's physical offices will ...Roast tenderloins on center rack of 350° oven for 20 minutes. Remove from oven and reprogram oven to broil, with oven rack positioned 5 1/2"-6" under heat. Using a pastry brush, paint a light coating of glaze on the surface of both tenderloins. Place under broiler for 3 minutes.Charcot-Marie-Tooth disease Videos, Flashcards, High Yield Notes, & Practice Questions. Learn and reinforce your understanding of Charcot-Marie-Tooth disease. - Osmosis is an efficient, enjoyable, and social way to learn. Sign up for an account today! Don't study it, Osmose it.Citation, DOI & article data. Müller-Weiss syndrome, also known as Brailsford disease 3, refers to spontaneous multifactorial adult onset osteonecrosis of the tarsal navicular. This syndrome is distinct from K öhler disease , the osteonecrosis of the tarsal navicular bone that occurs in children.Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger Anadolu Kardiyol Derg . 2012 Sep;12(6):523-4. doi: 10.5152/akd.2012.165. Cri du chat syndrome is a rare genetic disorder caused by a missing section on a particular chromosome known as Chromosome 5. Sometimes, material from another chromosome is missing as well. Around one in every 50,000 or so babies is diagnosed with this disorder. This estimate is coming down.Overview. CHARGE syndrome is a recognizable genetic syndrome with known pattern of features. It is an extremely complex syndrome, involving extensive medical and physical difficulties that differ from child to child. CHARGE syndrome is correlated with genetic mutation to CHD7 and the prevalence of CHARGE syndrome is 1:10,000-1:15,000 live births.The disorder mapping to chromosome 17 was referred to as Charcot-Marie-Tooth disease type 1A or hereditary motor and sensory neuropathy type I (HMSN I). In studies of 7 families, Chance et al. ( 1989, 1990) found a high probability of linkage to chromosome 17 markers in 5.Welcome to the ECMTF. The European Charcot-Marie-Tooth (aka CMT) Federation is a nonprofit organization created to unite all the CMT advocacy groups across Europe to help raise awareness and promote better care for people with Charcot-Marie-Tooth disease, a rare invalidating neuropathy, fund research and encourage the formation of new ... billiard factoryCharcot-Marie-Tooth disease (CMT) is known as a hereditary motor and sensory neuropathy (HMSN) and is the most common inherited neuromuscular disease with a prevalence of approximately 1 in every 2,500 [1].https://www.amazon.com/Mosbys-Medical-Dictionary-Mosby/dp/0323414257?&_encoding=UTF8&tag=maturecolors2-20Char syndromeChar syndrome: A genetic disorder chara...Char syndrome is inherited in an autosomal dominant manner. The proportion of cases caused by a de novo pathogenic variant is unknown. If a parent of the proband is affected, the risk to the sibs is 50%. When the parents are clinically unaffected, the risk to the sibs of a proband appears to be low.2020 Pokémon Sword And Shield Champions Path Vmax Rainbow Charizard BGS 9.5+ $298.00: Report It: 2022-03-27: Pokemon Brilliant Stars ... The prices shown are the lowest. Buy Charizard VMAX - 20/189 - Ultra Rare Sword & Shield: Darkness Ablaze Singles: Everything Else - Amazon.com FREE DELIVERY possible on eligible purchases. fedex photo printing prices; mitsubishi mirage sale; connect onn ... Diabetic (Charcot) Foot. Diabetes is a condition of elevated blood sugar that affects about 9% of the population in the United States, or about 30 million people. Diabetic foot problems are a major health concern and a common cause of hospitalization. Most foot problems that people with diabetes face arise from the damage that the disease ... kart o maniaChar syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger Anadolu Kardiyol Derg . 2012 Sep;12(6):523-4. doi: 10.5152/akd.2012.165. The Marfan Foundation's mission is to save lives and improve the quality of life of individuals with Marfan syndrome, Loeys-Dietz syndrome, Vascular Ehlers-Danlos syndrome (VEDS), and other genetic aortic and vascular conditions. Together, We are Fighting for Victory View all Divisions Marfan Foundation Loeys-Dietz Syndrome Foundation The VEDSCharcot-Marie syndrome synonyms, Charcot-Marie syndrome pronunciation, Charcot-Marie syndrome translation, English dictionary definition of Charcot-Marie syndrome. n. 1. A group of symptoms that collectively indicate or characterize a disease, disorder, or other condition considered abnormal. 2. a. A complex of...These specialists have recieved grants, written articles, run clinical trials, or taken part in organizations relating to Char syndrome, and are considered knowledgeable about the disease as a result. The people in this list are filtered based on their research related to Char syndrome, and as a result may or may not have a clinical practice. Citisli V. Assessment of diagnosis and treatment of thoracic outlet syndrome , an important reason of pain in upper extremity, based on literature. J Pain Relief ... The basic symptoms of a syndrome are revealed upon the direct observation of an afflicted individual; these symptoms may include stomach pain, vomiting, muscular tension in the anterior abdominal wall, and Blumberg's sign, which indicates peritoneal irritation with acute abdomen.Churg-Strauss syndrome is a disorder marked by blood vessel inflammation. This inflammation can restrict blood flow to organs and tissues, sometimes permanently damaging them. This condition is also known as eosinophilic granulomatosis with polyangiitis (EGPA). Adult-onset asthma is the most common sign of Churg-Strauss syndrome.Down syndrome is usually caused by an error in cell division called "nondisjunction." Nondisjunction results in an embryo with three copies of chromosome 21 instead of the usual two. Prior to or at conception, a pair of 21st chromosomes in either the sperm or the egg fails to separate.Chapter 87 PNS Demyelinating Disorders CHARCOT-MARIE-TOOTH DISEASE osms.it/Charcot-Marie-Tooth PATHOLOGY & CAUSES Group of hereditary, progressive neurological disorders; disruption of PNS processes, impaired sensory/motor function Genetic mutations → defective structure, function of proteins in myelin sheath/ neuron's axon Classification: Types I-VII; Type X (X-linked) Subtypes based ...Member types char_type, traits_type and allocator_type are the class template parameters of basic_stringstream. Return Value For (1), a basic_string object with a copy of the current contents in the stream buffer. Member types char_type, traits_type and allocator_type are the class template parameters of basic_stringstream. Example. local wells fargo xa