日本患者生殖器髌综合征在新生儿期短暂表现为心脏壁内腔。

Case Reports in Genetics Pub Date : 2020-08-29 eCollection Date: 2020-01-01 DOI:10.1155/2020/1731720
Kiichi Takahashi, Hiroyuki Adachi, Manatomo Toyono, Masato Ito, Akie Kato, Atsuko Noguchi, Tsutomu Takahashi
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摘要

生殖器髌骨综合征(GPS)是一种罕见的常染色体显性遗传病,由KAT6B基因的新发病变异引起。其特征为生殖器异常、髌骨发育不全、髋膝屈曲挛缩、胼胝体发育不全伴小头畸形、肾积水和/或多发肾囊肿。超过一半的GPS患者有先天性心脏缺陷,主要是心房和/或室间隔缺损、卵圆孔未闭和动脉导管未闭。我们报告一例日本新生儿与新杂合c.3769_3772delTCTA致病变异的KAT6B基因谁在出生时表现为室间隔心脏壁内腔。1月龄时腔体意外消失,但小梁间隔变薄和闪光仍然存在。该腔的特征与先天性室性憩室或动脉瘤不一致,其身份及预后尚不清楚。由于GPS患者可能表现出各种形式的心脏畸形,因此对于疑似GPS的患者,从出生起就需要进行仔细的心脏检查和随访。
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A Japanese Patient with Genitopatellar Syndrome Transiently Presenting with Cardiac Intramural Cavity during the Neonatal Period.

Genitopatellar syndrome (GPS) is a rare autosomal dominant disorder caused by de novo pathogenic variants in the KAT6B gene. It is characterized by genital abnormalities, patellar hypoplasia/agenesis, flexion contractures of the hips and knees, corpus callosum agenesis with microcephaly, and hydronephrosis and/or multiple renal cysts. More than half of patients with GPS have congenital heart defects, mostly atrial and/or ventricular septal defects, patent foramen ovale, and patent ductus arteriosus. We report a case of a Japanese neonate with a de novo heterozygous c.3769_3772delTCTA pathogenic variant in the KAT6B gene who presented with a cardiac intramural cavity of the ventricular septum at birth. The cavity unexpectedly disappeared at 1 month of age, but trabecular septal thinning and flash remained. The features of the cavity were not consistent with those of congenital ventricular diverticulum or aneurysm, and its identity and prognosis are still unclear. Because patients with GPS may exhibit various forms of cardiac malformation, careful cardiac examination and follow-up are required from birth in cases of suspected GPS.

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