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Category:Neurogenetic disorders

From WikiMD's medical encyclopedia

Pages in category "Neurogenetic disorders"

The following 21 pages are in this category, out of 21 total.

A

  • Allan–Herndon–Dudley syndrome

D

  • Glucose transporter type 1 deficiency syndrome
  • Hypertrophic neuropathy of Dejerine-Sottas
  • Dentatorubral–pallidoluysian atrophy

F

  • Fragile X syndrome

H

  • Hereditary neuropathies
  • Hereditary sensory and autonomic neuropathy
  • Hereditary sensory and autonomic neuropathy type 7
  • Hereditary sensory and autonomic neuropathy type V
  • Hereditary sensory neuropathy type 1

M

  • McLeod neuroacanthocytosis syndrome

P

  • Pontocerebellar hypoplasia
  • Pontocerebellar hypoplasia type 1
  • Pontocerebellar hypoplasia type 2
  • Pontocerebellar hypoplasia type 4
  • Pontocerebellar hypoplasia type 5
  • Pontocerebellar hypoplasia type 6

R

  • Roussy Levy syndrome

S

  • Spinal muscular atrophy
  • Spinal muscular atrophy 1

T

  • Tourette syndrome
Retrieved from "https://wikimd.org/w/index.php?title=Category:Neurogenetic_disorders&oldid=6175950"
Categories:
  • Genetic disorders by system
  • Congenital disorders of nervous system
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  • This page was last edited on 22 January 2025, at 17:34.
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