Autosomal dominant Charcot-Marie-Tooth neuropathy and deafness is a rare inherited nerve disease. In this condition, the long nerves to the feet and hands ...
Dr. Samantha A. Vergano, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist.
Charcot-Marie-Tooth disease type 1E (CMT1E) is a rare inherited nerve disease. It mainly harms the peripheral nerves, which are the long nerves that carry ...
Hereditary motor and sensory neuropathy 1D (HMSN 1D) is a rare, inherited nerve disease. It is the same condition as Charcot-Marie-Tooth disease type 1D ...
Charcot-Marie-Tooth neuropathy type 1D (CMT1D) is a rare, inherited nerve disease that mainly damages the long nerves going to the feet, legs, hands, and arms. ...
Charcot-Marie-Tooth disease type 1 caused by mutation in the EGR2 gene is a rare, inherited nerve disease that mainly affects the nerves of the arms and legs. ...
Charcot-Marie-Tooth disease type 1D (CMT1D) is a rare, inherited nerve disease. It mainly affects the “peripheral nerves”. These are the long nerves that carry ...
Charcot-Marie-Tooth slow nerve conduction type C is a rare inherited nerve disease that mainly affects the long nerves in the arms and legs. It belongs to the ...
Charcot-Marie-Tooth neuropathy type 1C (CMT1C) is a rare, inherited nerve disease. It mainly damages the peripheral nerves, which are the long nerves that ...
Charcot-Marie-Tooth disease type 1 caused by mutation in LITAF is usually called Charcot-Marie-Tooth disease type 1C (CMT1C). It is a rare, inherited nerve ...
Charcot-Marie-Tooth disease type 1C (CMT1C) is a rare, inherited nerve disease. It mainly affects the long nerves that control movement and feeling in the ...
Hereditary motor and sensory neuropathy IB (HMSN IB) is another name for Charcot–Marie–Tooth disease type 1B (CMT1B). It is a rare, inherited nerve disease ...
Hereditary motor and sensory neuropathy (HMSN) is a group of genetic nerve diseases where the nerves that control movement and feeling in the arms and legs ...
Charcot-Marie-Tooth neuropathy type 1B (CMT1B) is a rare, inherited nerve disease that mainly affects the peripheral nerves in the arms and legs. These nerves ...
Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ is a long-lasting, inherited nerve disease that mainly damages the nerves in the arms and legs. It ...
Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy is a hereditary nerve disease in which the outer covering of the nerves (myelin) is ...
Autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B (often shortened to CMT1B with focally folded myelin) is a rare ...
Charcot-Marie-Tooth disease type 1B (CMT1B) is a rare inherited nerve disease that mainly affects the nerves in the legs, feet, hands, and arms. These nerves ...
Hereditary motor and sensory neuropathy type 1A (HMSN 1A) is a genetic nerve disease that slowly damages the long nerves in the arms and legs. It mainly ...
Charcot-Marie-Tooth neuropathy type 1A (CMT1A) is an inherited nerve disease that mainly affects the nerves in the arms and legs. These nerves are called ...
Autosomal dominant Charcot–Marie–Tooth disease with focally folded myelin sheaths type 1A is a very rare form of Charcot–Marie–Tooth disease (CMT) type 1A. It ...
