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)

Cockayne Syndrome (Orthochromatic Leukodystrophy)

Familial Arrhiny with Peter's Anomaly

Hypertelorism

Mandibulo-Facial Dysplasia

Marfan's Syndrome

Noonan Syndrome

Progeria, Hutchinson-Gilford Syndrome

Progeria, Hutchison-Gilford Syndrome #1

Progeria, Hutchison-Gilford Syndrome #2

Weill-Marchesani Syndrome, Finger

Distúrbios da Motilidade Ocular e Estrabismo

Doenças Sistêmicas

Esclera

Glaucoma e Hipertensão Ocular

Hypertensive Retinopathy

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Progeria, Hutchison-Gilford Syndrome #2

Diagnosis:	Progeria, Hutchison-Gilford Syndrome #2
Comment to photo:
Author(s):	Woodward, Julie, M.D., Duke University Eye Center, Durham, NC, USA
ICD10-Code:	e34.8
Path:	Anomalias, Malformações e Síndromes Congênitas -> Síndromes Hereditárias -> Progeria, Hutchinson-Gilford Syndrome
Additional keywords:
Image ID:	7547

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