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一种具有明显X连锁隐性遗传的致死性多发性翼状胬肉综合征。

A lethal multiple pterygium syndrome with apparent X-linked recessive inheritance.

作者信息

Tolmie J L, Patrick A, Yates J R

机构信息

Duncan Guthrie Institute of Medical Genetics, Royal Hospital for Sick Children, Yorkhill, Glasgow, Scotland.

出版信息

Am J Med Genet. 1987 Aug;27(4):913-9. doi: 10.1002/ajmg.1320270418.

Abstract

We describe three male fetuses with a lethal multiple pterygium syndrome (LMPS). The family was ascertained when the first pregnancy of healthy, unrelated Scottish parents ended with a miscarriage at 23 weeks gestation. The macerated male fetus had a cystic hygroma, cleft palate, and webbing of the neck, elbows, and thighs. Radiographs showed lack of modeling of long bones, with broad ribs and clavicles, hypoplastic radii and ulnae, abnormal jaw angle, and dislocated femoral heads. Two other fetuses with similar anomalies were born to a first cousin of the propositus. These three male fetuses with a similar lethal multiple pterygium syndrome born to mothers who are second-degree relatives through the female line suggest X-linked recessive inheritance of LMPS in this family.

摘要

我们描述了三名患有致死性多发性翼状胬肉综合征(LMPS)的男性胎儿。该家族是在一对健康、无亲缘关系的苏格兰父母的首次妊娠于妊娠23周时以流产告终后被发现的。该浸软的男性胎儿有一个囊状水瘤、腭裂以及颈部、肘部和大腿的蹼状畸形。X线片显示长骨缺乏塑形,肋骨和锁骨宽阔,桡骨和尺骨发育不全,下颌角异常,股骨头脱位。另外两名有类似异常的胎儿是先证者的第一代堂表亲所生。这三名患有类似致死性多发性翼状胬肉综合征的男性胎儿,其母亲通过女性系为二级亲属,提示该家族中LMPS为X连锁隐性遗传。

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