Atlas of Ophthalmology

Anterior Chamber

Brain

Choroid

Congenital Syndromes

Albinism (see under Iris)

Anomalies of Eye Size

Chromosomal Anomalies

Malformation of the Optic Cup

Marcus Gunn Jaw-Winking

Syndromes

Apert's Syndrome (Acrocephalosyndactyly)

Arthrogryposis Syndrome

Bardet-Biedl Syndrome

Bloch-Sulzberger-Syndrome (Incontinentia Pigmenti)

Cockayne Syndrome (Orthochromatic Leukodystrophy)

Familial Arrhiny with Peters' Anomaly

Hypertelorism

Mandibulo-Facial Dysplasia

Marfan's Syndrome

Noonan Syndrome

Progeria

Progeria, Hutchison-Gilford症候群

Weill-Marchesani 症候群、指

基底細胞母斑症候群(Gorlin症候群）、顔面皮膚

Conjunctiva

Cornea

Glaucomas

Hypertensive Retinopathy

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Iris and Ciliary Body

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Progeria, Hutchison-Gilford症候群

Diagnosis:	Progeria, Hutchison-Gilford症候群
Comment to photo:	6ヵ月から3歳の間に本症候群の子供は年老い始める。毛髪は薄くなり、抜け始める。両眼の眼裂縮小と白内障を認める。高血圧、虚血性心疾患を早期から発症し、若くして死亡する。
Author(s):	Woodward, Julie, M.D., Duke University Eye Center, Durham, NC, USA
ICD10-Code:	e34.8
Path:	Congenital Syndromes -> Syndromes -> Progeria
Additional keywords:
Image ID:	7501

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