Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): Report of 16 fetal cases

Author:

Bessières-Grattagliano B.,Foliguet B.,Devisme L.,Loeuillet L.,Marcorelles P.,Bonnière M.,Laquerrière A.,Fallet-Bianco C.,Martinovic J.,Zrelli S.,Leticee N.,Cayol V.,Etchevers H.C.,Vekemans M.,Attie-Bitach T.,Encha-Razavi F.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference21 articles.

1. Congenital hydrocephalus-hydranencephaly in five siblings with autopsy studies: a new disease;Fowler;Dev. Med. Child. Neurol.,1972

2. Proliferative vasculopathy and an hydranencephalic hydrocephalic syndrome: a neuropathological study of two siblings;Harper;Dev. Med. Child. Neurol.,1983

3. Fetal neuropathology of proliferative vasculopathy and hydranencephaly-hydrocephaly with multiple limb pterygia;Norman;Ped Neurosc,1988

4. Autosomal recessive encephaloclastic proliferative vasculopathy (hydrocephaly/hydranencepahly);Moeschler;Am. J. Hum. Genet.,1989

5. The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly: immunohistochemical and ultrastructural evidence for endothelial proliferation;Harding;Neuropathol. Appl. Neurobiol.,1995

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