Back to Results
First PageMeta Content
Anatomy / Charcot–Marie–Tooth disease / Hereditary neuropathy with liability to pressure palsy / Dejerine–Sottas disease / Myelin / Peripheral myelin protein 22 / Peripheral neuropathy / Schwann cell / Chromosome 17 / Neurological disorders / Biology / Health


Charcot-Marie-Tooth Disease
Add to Reading List

Document Date: 2015-02-22 11:07:14

Open Document

File Size: 364,29 KB

Share Result on Facebook

Country

France / United States / United Kingdom / /

Currency

pence / /

IndustryTerm

manufacturing myelin protein zero / orthopedic devices / /

MedicalCondition

paralysis / Foot deformities / HMSN / X-linked disorder / Progressive muscle weakness / palsy / disease / common inherited neurological disorders / Marie-Tooth disease / Charcot-MarieTooth disease / Autosomal disorders / Charcot-Marie-Tooth disease / autosomal dominant disease / muscle weakness / hereditary motor / Dejerine-Sottas disease / hereditary neuropathy / X-linked dominant disease / severe muscle atrophy / cut / CMT experience tremor / peroneal muscular atrophy / rare disorder / disorder / Autosomal recessive disorders / demyelination / CMT disease / heterogenous genetic disease / chronic shortening / contractures / Nerve pain / scoliosis / disorders / /

Organization

U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES / DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service National Institutes of Health / /

Person

Howard Henry Tooth / Pierre Marie / Jean-Martin Charcot / /

Product

FS / /

Technology

genetic code / /

SocialTag