par Désir, Julie ;Abramowicz, Marc
Référence Orphanet journal of rare diseases, 3, page (28)
Publication Publié, 2008
Article révisé par les pairs
Titre:
  • Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome).
Auteur:Désir, Julie; Abramowicz, Marc
Informations sur la publication:Orphanet journal of rare diseases, 3, page (28)
Statut de publication:Publié, 2008
Sujet CREF:Sciences bio-médicales et agricoles
MeSH keywords:Adolescent
Adult
Audiometry
Child
Child, Preschool
Corneal Dystrophies, Hereditary -- diagnosis
Corneal Dystrophies, Hereditary -- genetics
Corneal Dystrophies, Hereditary -- physiopathology
Corneal Dystrophies, Hereditary -- surgery
Corneal Transplantation
Female
Hearing Loss, Sensorineural -- diagnosis
Hearing Loss, Sensorineural -- genetics
Hearing Loss, Sensorineural -- physiopathology
Hearing Loss, Sensorineural -- surgery
Humans
Male
Young Adult
Note générale:Journal Article
Research Support, Non-U.S. Gov't
Review
Langue:Anglais
Identificateurs:urn:issn:1750-1172
info:doi/10.1186/1750-1172-3-28
info:pii/1750-1172-3-28
info:scp/55149103495
info:pmid/18922146
PMC2576053