Charcot-Marie-Tooth disease caused by mutation in YARS is a very rare, inherited nerve disease that damages the long nerves to the feet, legs, hands, and arms. ...
Dr. Harun Ar Rashid, MD - Arthritis, Bones, Joints Pain, Trauma, and Internal Medicine Specialist
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (often shortened to AD-CMTD type C or CMTDIC) is a rare inherited nerve disease. It mainly ...
Charcot-Marie-Tooth disease dominant intermediate C (often shortened to DI-CMT C) is a very rare inherited nerve disease that slowly damages the long nerves of ...
Charcot-Marie-Tooth neuropathy, dominant intermediate B (often shortened to CMTDIB) is a very rare inherited nerve disease that mainly affects the long nerves ...
Charcot-Marie-Tooth disease, axonal type 2M (CMT2M), is a very rare inherited nerve disease that mainly damages the long “wires” of the body called peripheral ...
Charcot-Marie-Tooth disease dominant intermediate type B (often shortened to CMT-DIB) is a very rare, inherited nerve disease. It mainly affects the peripheral ...
Charcot-Marie-Tooth disease dominant intermediate 1 (CMTDI1) is a very rare inherited nerve disease that mainly affects the arms and legs. In this condition, ...
Charcot-Marie-Tooth disease caused by mutation in DNM2 is a rare, inherited nerve disease that slowly damages the long nerves of the arms and legs. These ...
Charcot-Marie-Tooth disease dominant intermediate B (often shortened to CMTDIB or DI-CMTB) is a very rare inherited nerve disease. It mainly damages the ...
Charcot-Marie-Tooth neuropathy type 2Z (CMT2Z) is a rare inherited nerve disease that mainly damages the long nerves of the legs and arms (peripheral nerves). ...
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 mutation is a rare inherited nerve disease that mainly damages the long “wires” (axons) of ...
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2Z (CMT2Z) is a rare hereditary nerve disease caused by harmful changes in the MORC2 gene. It mainly ...
Charcot-Marie-Tooth disease axonal type 2Z (CMT2Z) is a rare inherited nerve disease. It mainly damages the long nerves in the arms and legs (peripheral ...
Charcot-Marie-Tooth neuropathy type 2X (often grouped under X-linked Charcot-Marie-Tooth disease, or CMTX) is a rare inherited nerve disease that mainly ...
Charcot-Marie-Tooth disease caused by mutation in SPG11 is a very rare, inherited nerve disease. Doctors also call it autosomal recessive Charcot-Marie-Tooth ...
Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation (often called CMT2X due to SPG11) is a very rare inherited nerve disease that ...
Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 (spatacsin) mutation is a very rare inherited nerve disease. It mainly damages the long ...
Autosomal recessive axonal Charcot-Marie-Tooth disease type 2X (often written CMT2X or AR-CMT2X) is a rare inherited nerve disease where the long nerves in the ...
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (also called cerebellar hypoplasia–tapetoretinal degeneration syndrome) is a very ...
Cerebellar hypoplasia–tapetoretinal degeneration syndrome is a very rare condition where two main body parts are affected from early life: the cerebellum (a ...
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