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[以常染色体隐性模式遗传的中脑导水管先天性狭窄(2个家族中的5例)]

[Congenital stenosis of the aqueduct of Sylvius transmitted in an autosomal recessive mode (5 cases in 2 families)].

作者信息

Vanlieferinghen P, Chazal J, Francannet C, Malpuech G, Storme B

机构信息

Service de Pédiatrie B et Génétique Médicale, Hôtel-Dieu, CHRU Clermont-Ferrand.

出版信息

J Genet Hum. 1987 Aug;35(4):251-8.

PMID:3498797
Abstract

The authors report 5 cases of congenital hydrocephalus due to isolated stenosis of the aqueduct of Sylvius. In the first three cases (2 brothers and 1 sister) ventriculograms showed apparent obstruction of the aqueduct. A valve shunting was necessary at 1 month of age in cases 1 and 2, at 3 years of age in case 3. In cases 4 and 5 (1 brother and 1 sister) ultrasonic prenatal diagnosis showed ventriculomegaly and pregnancies were interrupted respectively at 31 and 28 weeks of gestational age. The pedigree of the families suggests that the inheritance of this abnormality is autosomal recessive. Such an inheritance is very unusual and confirms the difficulty of genetic counseling facing the first occurrence of hydrocephalus with stenosis of the aqueduct of Sylvius in a family. The prenatal diagnosis is based on fetal ultrasonic examination and may be obtained late in the pregnancy leading to therapeutic and ethical tricky decisions.

摘要

作者报告了5例因中脑导水管孤立性狭窄导致的先天性脑积水病例。在前3例(2兄弟和1姐妹)中,脑室造影显示导水管明显梗阻。病例1和病例2在1月龄时需要进行瓣膜分流,病例3在3岁时进行。在病例4和病例5(1兄弟和1姐妹)中,产前超声诊断显示脑室扩大,分别在孕31周和28周时终止妊娠。这些家庭的系谱表明,这种异常的遗传方式为常染色体隐性遗传。这种遗传方式非常罕见,证实了对于一个家庭中首次出现中脑导水管狭窄性脑积水时进行遗传咨询的困难。产前诊断基于胎儿超声检查,可能在妊娠晚期才能做出,这会导致治疗和伦理方面棘手的决策。

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