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9号染色体三体综合征两例非典型表现:对发育迟缓的重新思考

Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay.

作者信息

Saneto R P, Applegate K E, Frankel D G

机构信息

Department of Pediatric Neurology, Cleveland Clinic Foundation and Children's Hospital, Ohio 44195, USA.

出版信息

Am J Med Genet. 1998 Oct 30;80(1):42-5.

PMID:9800910
Abstract

Trisomy 9 syndrome is characterized by "bulbous" nose, microphthalmia, dislocated limbs, and other anomalies of skeletal, cardiac, genitourinary, and central nervous systems. With the exception of one reported case study, all surviving infants have had severe mental impairment. The prospect of severe mental retardation often overwhelms parents who are faced with prenatal diagnosis of trisomy 9. We report on two new cases of mosaic trisomy 9, both of whom are only mildly developmentally delayed. One patient presented with the distinctive facial appearance, large fontanels, and joint abnormalities. The other had none of the typical congenital abnormalities. However, the patient was found to have a congenital heart defect and hypoplastic left heart syndrome, which to our knowledge has not been reported previously in the trisomy 9 syndrome. When these two patients are added to the published patients with this syndrome, there appears to be a range of manifestations, especially with respect to mental status, which has not fully been recognized.

摘要

9号染色体三体综合征的特征包括“球根状”鼻子、小眼畸形、肢体脱位以及骨骼、心脏、泌尿生殖系统和中枢神经系统的其他异常。除了一篇报道的病例研究外,所有存活的婴儿都有严重的智力障碍。严重智力发育迟缓的前景常常使面临9号染色体三体产前诊断的父母不堪重负。我们报告了两例新的9号染色体嵌合三体病例,这两名患者都只有轻度发育迟缓。一名患者表现出独特的面部外观、大囟门和关节异常。另一名患者没有典型的先天性异常。然而,该患者被发现患有先天性心脏病和左心发育不全综合征,据我们所知,这在9号染色体三体综合征中以前尚未有过报道。当将这两名患者加入到已发表的该综合征患者中时,似乎存在一系列表现,尤其是在精神状态方面,这尚未得到充分认识。

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