Atlas of Ophthalmology

Anterior Chamber

Brain and Optical Pathway

Congenital Syndromes, Malformations and Abnomalities

Abnormalities/Anomalies of Eye Size

Chromosomal Abnormalities/Anomalies

Congenital Malformation of Nervous System

Hereditary Pigment Anomalies

Hereditary Syndromes

Acrocephalodactyly

Arthrogryposis Syndrome

Bardet-Biedl Syndrome

Basal-Cell Nevus Syndrome (Gorlin Syndrome), Skin of Face

Bloch-Sulzberger Syndrome (Incontinentia Pigmenti)

Cockayne Syndrome (Orthochromatic Leukodystrophy)

Familial Arrhiny with Peter's Anomaly

Mandibulo-Facial Dysplasia

Marfan's Syndrome

Noonan Syndrome

Progeria, Hutchinson-Gilford Syndrome

Weill-Marchesani Syndrome, Finger

Malformation of the Optic Cup

Glaucomas, Ocular Hypertension

Hypertensive Retinopathy

Iris and Ciliary Body

Lacrimal System

Neuro-Ophthalmology

Strabismus, Ocular Motility Disorders

Systemic Diseases

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Basal-Cell Nevus Syndrome (Gorlin Syndrome), Skin of Face

Diagnosis:	Basal-Cell Nevus Syndrome (Gorlin Syndrome), Skin of Face
Comment to photo:	Multiple basal-cell epitheliomas (in this case on the skin of the face). split ribs and cysts of the maxilla and mandibula. Autosomal dominant inheritance
Author(s):	Ruprecht, Klaus, Prof. Dr. med., Universitäts-Augenklinik, Homburg/Saar, Germany
ICD10-Code:	Q84.9, Q82.9
Path:	Congenital Syndromes, Malformations and Abnomalities -> Hereditary Syndromes
Additional keywords:	congenital syndrome, skin, tumor
Image ID:	3895

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