Atlas of Ophthalmology

眼前房

Brain

Hypertensive Retinopathy

iPod 稿件

Z Videos

先天综合征、畸形

Marcus Gunn综合征（下颌瞬目综合征）

先天性视杯发育异常

各种综合征

Apert's Syndrome (Acrocephalosyndactyly)

Arthrogryposis Syndrome

Bardet-Biedl Syndrome

Basal Cell Nevus Syndrome, Skin of Face

Bloch-Sulzberger-Syndrome (Incontinentia Pigmenti)

Cockayne Syndrome (Orthochromatic Leukodystrophy)

Familial Arrhiny with Peters' Anomaly

Hypertelorism

Mandibulo-Facial Dysplasia

Marfan's Syndrome

Noonan Syndrome

Progeria

儿童早衰症，Hutchison-Gilford综合症#1.

儿童早衰症，Hutchison-Gilford综合症#2.

Weill-Marchesani Syndrome, Finger

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儿童早衰症，Hutchison-Gilford综合症#1.

Diagnosis:	儿童早衰症，Hutchison-Gilford综合症#1.
Comment to photo:	在6个月至3岁间，儿童看上去开始衰老。头发脱落变薄。双侧的睑裂狭小，白内障。患有高血压和缺血性心脏病，往往早期死亡。
Author(s):	Woodward, Julie, M.D., Duke University Eye Center, Durham, NC, USA
ICD10-Code:	e34.8
Path:	先天综合征、畸形 -> 各种综合征 -> Progeria
Additional keywords:
Image ID:	7501

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