Atlas of Ophthalmology

Anomalias, Malformações e Síndromes Congênitas

Anomalias Hereditárias da Pigmentação

Anormalidades do Tamanho do Olho

Anormalidades/Anomalias Cromossômicas

Malformação do Disco Óptico

Malformações Congênitas do Sistema Nervoso

Síndromes Hereditárias

Acrocephalodactyly

Arthrogryposis Syndrome

Bardet-Biedl Syndrome

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

Bloch-Sulzberger Syndrome (Incontinentia Pigmenti)

Incontinentia Pigmenti (#1) Skin (Bloch-Sulzberger Syndrome)

Incontinentia Pigmenti (#2), (Bloch-Sulzberger Syndrome)

Incontinentia Pigmenti (#3), (Bloch-Sulzberger Syndrome)

Incontinentia Pigmenti (#4), (Bloch-Sulzberger Syndrome)

Incontinentia Pigmenti (Bloch-Sulzberger)

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

Distúrbios da Motilidade Ocular e Estrabismo

Doenças Sistêmicas

Esclera

Glaucoma e Hipertensão Ocular

Hypertensive Retinopathy

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Incontinentia Pigmenti (Bloch-Sulzberger)

Diagnosis:	Incontinentia Pigmenti (Bloch-Sulzberger)
Comment to photo:
Author(s):	Lommatzsch, Peter, Prof. Dr. med., Univ.-Augenklinik, Leipzig, Germany
ICD10-Code:	H18.08, Q82.3
Path:	Anomalias, Malformações e Síndromes Congênitas -> Síndromes Hereditárias -> Bloch-Sulzberger Syndrome (Incontinentia Pigmenti)
Additional keywords:	congenital syndromes
Image ID:	6002

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