Literature DB >> 1494731

[Systematized cavernous angiomatosis with multiple cerebral and cutaneous localizations].

F Bartolomei1, P Lemarquis, A Alicherif, A Lepillouer-Prost, J Sayag, R Khalil.   

Abstract

A 45 year-old woman with no history of familial disease presented with multiple cutaneous and cerebral cavernous angiomas. The diagnosis rested on biopsy for cutaneous angiomas and on MRI for cerebral angiomas. The clinical manifestations of cerebral angiomas were headaches and a cerebellar syndrome, the latter most probably due to progressive growth of cerebellar angiomas. Systematized cavernous angiomatosis is characterized by multiple angiomas of the brain and other viscera and is considered to be a phacomatosis.

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Year:  1992        PMID: 1494731

Source DB:  PubMed          Journal:  Rev Neurol (Paris)        ISSN: 0035-3787            Impact factor:   2.607


  2 in total

1.  Cutaneous venous malformations related to KRIT1 mutation: case report and literature review.

Authors:  Francesca Romana Grippaudo; Maria Piane; Matteo Amoroso; Benedetto Longo; Silvana Penco; Luciana Chessa; Maria Giubettini; Fabio Santanelli
Journal:  J Mol Neurosci       Date:  2013-07-05       Impact factor: 3.444

2.  Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutations.

Authors:  Agustí Toll; Elisabet Parera; Ana M Giménez-Arnau; Alejandro Pou; Josep Lloreta; Nisha Limaye; Miikka Vikkula; Ramon M Pujol
Journal:  Dermatology       Date:  2009-01-31       Impact factor: 5.366

  2 in total

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