📂 Diseases
hereditary sensory and autonomic neuropathy type 8 — Definition
kalıtsal duyusal ve otonom nöropati tip 8 / hereditary sensory and autonomic neuropathy type 8
Neuropathic pain is a rare genetic disease characterized by insensitiveness and anhydrous (healing), autozomal resessive transition. The result of mutations in the NTRK1 gene leads to dysfunction of the nervous growth factor receptor. Recurrent painless fractures in patients, neuropathic joints (Charcot joint) and delay in wound healing. Due to the arrest of the autonomous nervous system, the body temperature can not be arranged and hypertension attacks may occur.
Frequently Asked Questions
❓ What is kalıtsal duyusal ve otonom nöropati tip 8?
kalıtsal duyusal ve otonom nöropati tip 8; neuropathic pain is a rare genetic disease characterized by insensitiveness and anhydrous (healing), autozomal resessive transition. The result of mutations in the NTRK1 gene leads to dysfunction of the nervous growth factor receptor. Recurrent painless fractures in patients, neuropathic joints (Charcot joint) and delay in wound healing. Due to the arrest of the autonomous nervous system, the body temperature can not be arranged and hypertension attacks may occur.
❓ What is hereditary sensory and autonomic neuropathy type 8 in Turkish?
The Turkish equivalent of "hereditary sensory and autonomic neuropathy type 8" is kalıtsal duyusal ve otonom nöropati tip 8.
❓ Which medical field is kalıtsal duyusal ve otonom nöropati tip 8 related to?
This term belongs to the Diseases category.