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一名患有部分单侧隐眼畸形和多种先天性异常儿童的康复治疗

Rehabilitation of a child with partial unilateral cryptophthalmos and multiple congenital anomalies.

作者信息

Konrad H, Merriam J C, Jones I S

机构信息

Edward S. Harkness Eye Institute, College of Physicians and Surgeons, Columbia University, New York, USA.

出版信息

Trans Am Ophthalmol Soc. 1995;93:219-40; discussion 241-4. doi: 10.1016/s0002-9394(14)70557-4.

Abstract

PURPOSE

This paper describes the surgical rehabilitation of a child with craniofacial anomalies, unilateral syndactyly, and partial unilateral cryptophthalmos associated with inferior colobomata of the iris and optic nerve and agenesis of the inferior rectus and inferior oblique muscles. The clinical presentation of cryptophthalmos is described.

METHODS

The medical literature since the original description of cryptophthalmos in 1872 was reviewed to define patterns of inheritance and the incidence of associated anomalies.

RESULTS

Including this patient, 149 case reports of cryptophthalmos were identified. In two families transmission from parent to child suggests dominant inheritance. None of the five dominant cases had any other anomalies, and all had bilateral complete cryptophthalmos. The incidence of cryptophthalmos in the remaining families is consistent with autosomal recessive inheritance. This group includes patients with bilateral, unilateral, and partial cryptophthalmos. Other anomalies are common, including those of the ear and nose, limbs, genitourinary system, and mouth and palate. Mortality in the perinatal period is associated with renal agenesis, laryngeal atresia, and pulmonary hypoplasia.

CONCLUSIONS

Cryptophthalmos is a rare congenital anomaly with two patterns of inheritance.

摘要

目的

本文描述了一名患有颅面畸形、单侧并指畸形以及伴有虹膜和视神经下方缺损及下直肌和下斜肌发育不全的部分单侧隐眼畸形患儿的手术康复情况。文中描述了隐眼畸形的临床表现。

方法

回顾了自1872年首次描述隐眼畸形以来的医学文献,以确定其遗传模式及相关异常的发生率。

结果

包括该患者在内,共确定了149例隐眼畸形病例报告。在两个家族中,父母向子女的遗传提示为显性遗传。5例显性病例均无其他异常,且均为双侧完全性隐眼畸形。其余家族中隐眼畸形的发生率符合常染色体隐性遗传。该组包括双侧、单侧和部分隐眼畸形患者。其他异常很常见,包括耳、鼻、四肢、泌尿生殖系统以及口和腭的异常。围生期死亡率与肾发育不全、喉闭锁和肺发育不全有关。

结论

隐眼畸形是一种罕见的先天性异常,有两种遗传模式。

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