Suppr超能文献

患有CHARGE综合征的患者出现18三体。

Trisomy 18 in a patient with CHARGE association.

作者信息

Lee W T, Hou J W, Yau K I, Wang T R

机构信息

Department of Pediatrics, National Taiwan University Hospital, Taipei, R.O.C.

出版信息

J Formos Med Assoc. 1995 Jan-Feb;94(1-2):60-2.

PMID:7613237
Abstract

CHARGE association is the non-random association of congenital anomalies, including colobomata of the eyes, heart defects, choanal atresia, retardation of growth and development, genital hypoplasia and ear abnormalities. It is usually a sporadic event of unknown cause. We report a neonate with trisomy 18 and apparent CHARGE association. The associated abnormalities made the diagnosis difficult until the chromosomal results became available. Abnormalities such as clenched hands and short palpebral fissures pointed to the possibility of a chromosomal anomaly. The chromosome study revealed trisomy 18. It is important to perform chromosomal studies quickly when diagnosing a patient with apparent CHARGE association who also has other minor anomalies atypical of CHARGE.

摘要

CHARGE综合征是一种先天性异常的非随机关联,包括眼部缺损、心脏缺陷、后鼻孔闭锁、生长发育迟缓、生殖器发育不全和耳部异常。它通常是一种病因不明的散发性事件。我们报告一名患有18三体综合征且明显伴有CHARGE综合征的新生儿。在染色体检查结果出来之前,相关的异常情况使得诊断变得困难。诸如握拳和睑裂短小等异常提示了染色体异常的可能性。染色体研究显示为18三体。对于诊断为明显的CHARGE综合征且伴有其他非CHARGE典型的轻微异常的患者,快速进行染色体检查很重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验