MICRODELETION OF CHROMOSOME 7P SYNDROME OCULAR MANIFESTATIONS

被引：2

作者：

CARTWRIGHT, MJ ^{[1
]}

HASSAN, TS ^{[1
]}

FRUEH, BR ^{[1
]}

机构：

[1] UNIV MICHIGAN,WK KELLOGG EYE CTR,ANN ARBOR,MI 48105

来源：

OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY | 1995年 / 11卷 / 02期

关键词：

CHROMOSOMES; CHROMOSOME; 7; DELETION; DYSMORPHIC FEATURES; MYOGENIC PTOSIS; FRONTALIS SLING;

D O I：

10.1097/00002341-199506000-00012

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

Several syndromes have been associated with microdeletions of the autosomes. These syndromes are diverse in their morphology and frequently manifest abnormalities of the ocular adnexa. A child with an uncommon microdeletion of the short arm of chromosome 7P presented initially with congenital myogenic ptosis. After multiple systemic abnormalities were found during a routine examination, the child was referred for genetic evaluation where the defects were incidentally found. The child responded well with a fascia lata frontalis sling. The genetic disorder is discussed with an emphasis on the ophthalmologic findings.

引用

页码：139 / 141

页数：3

共 13 条

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