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HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)

Known as: CMT2C, HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC, CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C 
National Institutes of Health

Related topics

Related topics

14 relations
Abducens Nerve DiseasesAutosomal dominant inheritanceFootdropHammer Toe

Broader (1)

Charcot-Marie-Tooth Disease

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
PROCEEDINGS OF THE XVIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: Genoa, Italy June 6-9, 2018.
Congenital myotonic dystrophy (CMD) is a slowlyprogressive multisystemic disorder that presents in an wide spectrum of clinical… 
2011
2011
Clinical, laboratory, and genetic studies of families with Charcot-Marie-Tooth type 2C disease
Charcot-Marie-Tooth disease type 2C (CMT2C) is an autosomal dominant neuropathy characterized by limb, diaphragm, and laryngeal… 
Highly Cited
2003
Highly Cited
2003
The gene for HMSN2C maps to 12q23-24
Background: Hereditary motor and sensory neuropathy type 2C (HMSN2C, Charcot–Marie–Tooth 2C [CMT2C]) is an autosomal dominant… 
2000
2000
CHARCOT‐MARIE‐TOOTH WITH DIAPHRAGM AND VOCAL CORD PARALYSIS (CMT2C)
Charcot-Marie-Tooth disease (CMT) is the most common inherited disorder of the peripheral nervous system and is clinically and… 
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