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由于母亲生殖腺嵌合导致的家族性弯肢性发育不良。

Familial campomelic dysplasia due to maternal germinal mosaicism.

作者信息

Higeta Daisuke, Yamaguchi Rie, Takagi Takeshi, Nishimura Gen, Sameshima Kiyoko, Saito Kayoko, Minegishi Takashi

机构信息

Department of Obstetrics and Gynecology, Gunma University, Graduate School of Medicine, Gunma, Japan.

Department of Obstetrics and Gynecology, Japan Community Health Care Organization, Gunma Chuo Hospital, Gunma, Japan.

出版信息

Congenit Anom (Kyoto). 2018 Nov;58(6):194-197. doi: 10.1111/cga.12279. Epub 2018 Apr 2.

Abstract

Campomelic dysplasia is an autosomal dominant skeletal dysplasia caused by heterozygous SOX9 mutations. Most patients are sporadic due to a de novo mutation. Familial campomelic dysplasia is very rare. We report on a familial campomelic dysplasia caused by maternal germinal mosaicism. Two siblings showed the classic campomelic dysplasia phenotype with a novel SOX9 mutation (NM_000346.3: c.441delC, p.(Asn147Lysfs*36)). Radiological examination of the mother showed mild skeletal changes. Then, her somatic mosaicism of the mutation was ascertained. This is the first report of molecularly confirmed maternal germinal mosaicism for a SOX9 mutation. We suggest that a meticulous clinical examination of the parents, even if they are superficially healthy, is needed to avoid overlooking germinal mosaicism of SOX9 mutations.

摘要

弯肢侏儒症是一种由杂合性SOX9基因突变引起的常染色体显性骨骼发育不良。由于新发突变,大多数患者为散发病例。家族性弯肢侏儒症非常罕见。我们报告了一例由母源性生殖腺嵌合引起的家族性弯肢侏儒症。两名兄弟姐妹表现出典型的弯肢侏儒症表型,并伴有一个新的SOX9突变(NM_000346.3:c.441delC,p.(Asn147Lysfs*36))。对母亲的放射学检查显示有轻微的骨骼变化。随后,确定了她的体细胞突变嵌合现象。这是第一例分子学证实的母源性生殖腺SOX9基因突变嵌合的报告。我们建议,即使父母表面健康,也需要对其进行细致的临床检查,以避免忽视SOX9基因突变的生殖腺嵌合现象。

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