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一位患有18号染色体短臂三体的母亲所生的患有18号染色体短臂四体的同胞。

Sibs with tetrasomy 18p born to a mother with trisomy 18p.

作者信息

Takeda K, Okamura T, Hasegawa T

机构信息

Department of Paediatrics, Yuri-Kumiai General Hospital, Honjo, Japan.

出版信息

J Med Genet. 1989 Mar;26(3):195-7. doi: 10.1136/jmg.26.3.195.

Abstract

We report a family with an 18p trisomic mother and two 18p tetrasomic daughters. The mother is phenotypically normal and healthy, but with an unusual type of trisomy 18p: 47,XX,del(18)(pter----p11.21),+i(18p) de novo. The older sister has microcephaly, mental retardation, an asymmetrical and peculiar face with low set ears, pinched up nose, high arched palate, small mouth, micrognathia, tapering fingers, asymmetrical length of legs, and an asthenic body. The younger sister was stillborn with extensive defects of the skull, congenital hydrocephalus, severe facial anomalies, and lumbosacral meningocele. Both daughters have inherited one normal chromosome 18 and an isochromosome 18p from their mother, and one normal chromosome 18 from their father. Although one quite similar family has been reported, to the best of our knowledge there have been no reports of families in which two daughters with tetrasomy 18p syndrome have been born to a mother with trisomy 18p with isochromosomes.

摘要

我们报告了一个家庭,母亲为18号染色体短臂三体,两个女儿为18号染色体短臂四体。母亲表型正常且健康,但患有一种不寻常的18号染色体短臂三体类型:47,XX,del(18)(pter----p11.21),+i(18p) ,为新发突变。姐姐患有小头畸形、智力发育迟缓、面容不对称且奇特,耳朵低位、鼻子塌陷、腭弓高、嘴巴小、小颌畸形、手指细长、双腿长度不对称以及身体虚弱。妹妹为死产,有广泛的颅骨缺陷、先天性脑积水、严重的面部畸形和腰骶部脊膜膨出。两个女儿都从母亲那里遗传了一条正常的18号染色体和一条18号染色体短臂等臂染色体,从父亲那里遗传了一条正常的18号染色体。尽管已经报道了一个非常相似的家庭,但据我们所知,尚无关于母亲为18号染色体短臂三体并带有等臂染色体而生育两个患有18号染色体短臂四体综合征女儿的家庭的报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f08/1015583/e1aa82130b08/jmedgene00053-0051-a.jpg

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