Atlas of Ophthalmology

Anterior Chamber

Brain and Optical Pathway

Choroid

Congenital Syndromes, Malformations and Abnomalities

Abnormalities/Anomalies of Eye Size

Chromosomal Abnormalities/Anomalies

Congenital Malformation of Nervous System

Hereditary Pigment Anomalies

Hereditary Syndromes

Acrocephalodactyly

Apert's Syndrome

Apert's Syndrome, (Acrocephalosyndactyly)Face

Crouzon's Syndrome

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

Hypertelorism

Mandibulo-Facial Dysplasia

Marfan's Syndrome

Noonan Syndrome

Progeria, Hutchinson-Gilford Syndrome

Weill-Marchesani Syndrome, Finger

Malformation of the Optic Cup

Conjunctiva

Cornea

Glaucomas, Ocular Hypertension

Hypertensive Retinopathy

Iris and Ciliary Body

Strabismus, Ocular Motility Disorders

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Apert's Syndrome, (Acrocephalosyndactyly)Face

Diagnosis:	Apert's Syndrome, (Acrocephalosyndactyly)Face
Comment to photo:	Flat orbit, Exophthalmus, hypertelorism, exotropia, optic atrophy. Syndactyly. Autosomal dominant inheritance.
Author(s):	Ruprecht, Klaus, Prof. Dr. med., Universitäts-Augenklinik, Homburg/Saar, Germany
ICD10-Code:	Q87.0
Path:	Congenital Syndromes, Malformations and Abnomalities -> Hereditary Syndromes -> Acrocephalodactyly -> Apert's Syndrome
Additional keywords:	congenital syndromes
Image ID:	3888

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