Login / Signup

Hypotrichosis with cone-rod dystrophy in a patient with cadherin 3 (CDH3) mutation.

Fadi NasserL MulahasanovicM AlkhateebS BiskupK StinglE Zrenner
Published in: Documenta ophthalmologica. Advances in ophthalmology (2019)
This case shows that a CDH3 mutation besides macula dystrophy can cause widespread cone-rod dystrophy with hypotrichosis without any other pathology besides hypoplastic nails. This points to a common pathway of hair growth and photoreceptor development that can be disturbed by a CDH3 mutation (c.1508G>A; p.Arg503His) located in the EC4 repeat region of the gene.
Keyphrases
  • early onset
  • dna methylation