Congenital alacrima in a patient with G (Opitz Frias) syndrome

Congenital alacrima is an autosomal dominant disorder showing markedly deficient lacrimation and punctate corneal epithelial erosions. The G (Opitz-Frias) syndrome is also an autosomal dominant disorder characterised by hypertelorism, hypospadias, stridor, and dysphagia. Here we report a 5-year-old...

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Veröffentlicht in:	Human genetics 1996-04, Vol.97 (4), p.540-542
Hauptverfasser:	DUNDAR, M, ERKILIC, K, DEMIRYILMAZ, F, KÜCÜKAYDIN, M, KENDIRCI, M, OKUR, H, KAZEZ, A
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple Biological and medical sciences Child, Preschool Esophagus - abnormalities Face - abnormalities Humans Lacrimal Apparatus - abnormalities Larynx - abnormalities Male Malformations of the eye Medical sciences Ophthalmology Syndrome
Online-Zugang:	Volltext
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