Charcot-Marie-Tooth disease

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  • noun

Synonyms for Charcot-Marie-Tooth disease

a form of neuropathy that can begin between childhood and young adulthood

References in periodicals archive ?
Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4).
Haij: Top line results from our ongoing pivotal Phase 3 trial evaluating PXT3003 for the treatment of Charcot-Marie-Tooth disease type 1A (CMT1A) in adults are expected in the second quarter of 2018.
Hand involvement in children with Charcot-Marie-Tooth disease type 1A.
The phosphoinositide-3phosphatase MTMR2 associates with MTMR13, a membrane-associated pseudophosphatase also mutated in type 4B Charcot-Marie-Tooth disease.
The report reviews key players involved in the therapeutics development for Charcot-Marie-Tooth Disease and enlists all their major and minor projects
Following 15 years of intense research to understand the cause and to develop experimental models for hereditary neuropathies such as Charcot-Marie-Tooth disease, Professor Kleopas Kleopa, head of the Neuroscience Laboratory, along with a team of researchers, announced a successful gene delivery method targeting peripheral nerves to reverse the findings of neuropathy.
Keywords: Charcot-Marie-Tooth disease Peroneal dystrophy Ascorbic acid Nerve conduction velocity Demyelintion.
An inkling that fusion might be important for the normal muscle function came from research on two mitochondrial diseases: Autosomal Dominant Optical Atropy (ADOA) disease, and a type of Charcot-Marie-Tooth disease (CMT).
Charcot-Marie-Tooth disease subtypes and genetic testing strategies.
AROUND 23,000 people in the UK are currently living with Charcot-Marie-Tooth disease, or CMT, and it affects hundreds of thousands more worldwide.
Microvascular decompression for trigeminal neuralgia in Charcot-Marie-Tooth disease.
In the case of the individual with Charcot-Marie-Tooth disease reported on last year (N.
The two new lines would be the only lines on the federal registry to carry the genes for hemophilia B and Charcot-Marie-Tooth disease.
Hereditary peripheral neuropathies were described in 1886 by Tooth in the United Kingdom and by Charcot and Marie in France; hence, the disorders are known as Charcot-Marie-Tooth disease (CMT).
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