Alezzandrini syndrome (Q105016): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
Property / CURIE
 
CID11:ID_257912122
Property / CURIE: CID11:ID_257912122 / rank
 
Normal rank

Revision as of 10:55, 17 August 2026

A rare syndrome characterised by the development of unilateral retinal degeneration with ipsilateral facial vitiligo, poliosis and hearing loss.
Language Label Description Also known as
default for all languages
ID_257912122
    English
    Alezzandrini syndrome
    A rare syndrome characterised by the development of unilateral retinal degeneration with ipsilateral facial vitiligo, poliosis and hearing loss.

      Statements

      CID11:ID_257912122
      0 references