📂 Diseases
Charcot-Marie-Tooth disease type 1D — Definition
Charcot-Marie-Tooth hastalığı tip 1D / Charcot-Marie-Tooth disease type 1D
Charcot-Marie-Tooth disease type 1D is a hereditary neuropathic that affects the peripheral nervous system. This disease leads to weakness, sense loss and muscle melt especially on legs and feet. Type 1D shows autozomal dominant transition and is caused by mutations in EGR2 gene. Clinically, patients often refer to walking power during childhood or puberty, foot drop and reflex loss.
Frequently Asked Questions
❓ What is Charcot-Marie-Tooth hastalığı tip 1D?
Charcot-Marie-Tooth hastalığı tip 1D; charcot-Marie-Tooth disease type 1D is a hereditary neuropathic that affects the peripheral nervous system. This disease leads to weakness, sense loss and muscle melt especially on legs and feet. Type 1D shows autozomal dominant transition and is caused by mutations in EGR2 gene. Clinically, patients often refer to walking power during childhood or puberty, foot drop and reflex loss.
❓ What is Charcot-Marie-Tooth disease type 1D in Turkish?
The Turkish equivalent of "Charcot-Marie-Tooth disease type 1D" is Charcot-Marie-Tooth hastalığı tip 1D.
❓ Which medical field is Charcot-Marie-Tooth hastalığı tip 1D related to?
This term belongs to the Diseases category.