-- Collaboration to explore role of HDAC6 in multiple forms of CMT disease ---- Company appoints Dr. David Herrmann to Scientific Advisory Board -- WALTHAM, Mass.--(BUSINESS WIRE)--Regenacy ...
Purpose: An evidence-based approach was used to determine the frequency distribution of genes contributing to the Charcot-Marie-Tooth (CMT) disease phenotype. Methods: We performed a combined analysis ...
The hereditary motor and sensory neuropathies (HMSNs) are a clinically heterogeneous group of peripheral neuropathies, characterized by slowly progressive weakness and atrophy of the distal limb ...
Charcot-Marie-Tooth Disease is a family of inherited disorders of the peripheral nervous system, affecting approximately one in 2,500 Americans. Its most common iteration, CMT1, comes in many forms, ...
A new, inexpensive urine test that measures two sugar alcohols, sorbitol and xylitol, is making it easier, faster, and far less expensive to identify a common inherited nerve disorder called ...
GeneDx’s Hereditary Neuropathy Panel will be available free of charge to individuals at risk for or suspected of having GAN Taysha will collaborate with Hereditary Neuropathy Foundation and ...
Inherited mutations in a gene that keeps nerve cells intact was shown, for the first time, to be a driver of a neuropathy known as Charcot-Marie-Tooth disease. This finding presents a clearer picture ...
Q. My son has diabetes, and as a result, many problems with his feet. He has had to have surgical implants, has Charcot neuropathy in the left foot and has had three toes amputated on the right foot, ...
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