Mueller R F, Buckler J, Arthur R, Bonsor G, Dear P, Walters K, Towns G M
Department of Clinical Genetics, General Infirmary, Leeds, Belmont, Grove.
J Med Genet. 1992 Jun;29(6):425-7. doi: 10.1136/jmg.29.6.425.
We describe a child with typical features of the 3-M syndrome who presented with acute hydrocephalus owing to haemorrhage from one of two intracranial cerebral vascular aneurysms. We suggest that other children with this disorder should be screened for similar complications.
我们描述了一名患有3-M综合征典型特征的儿童,该儿童因颅内两个脑血管动脉瘤之一出血而出现急性脑积水。我们建议应对患有这种疾病的其他儿童进行类似并发症的筛查。