Literature DB >> 9435781

A new 3C syndrome: cerebellar hypoplasia, cavernous haemangioma and coarctation of the aorta.

W H Goh1, R Lo.   

Abstract

Two children were identified with facial haemangioma, cerebellar hypoplasia and co-arctation of the aorta; the second child presented to the neurology department because of facial haemangioma. The importance of awareness of the association of these three conditions is essential to ensure proper management and survival of this group of patients. The possible pathophysiology of these associated conditions is discussed.

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Year:  1993        PMID: 9435781     DOI: 10.1111/j.1469-8749.1993.tb11702.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  3 in total

1.  A report of two cases with dolichosegmental intracranial arteries as a new feature of PHACES syndrome.

Authors:  Carlos E Baccin; Timo Krings; Hortensia Alvarez; Augustin Ozanne; Pierre L Lasjaunias
Journal:  Childs Nerv Syst       Date:  2006-10-13       Impact factor: 1.475

2.  Facial haemangioma, agenesis of the internal carotid artery and dysplasia of cerebral cortex: case report.

Authors:  I Pascual-Castroviejo; J Viaño; S I Pascual-Pascual; V Martinez
Journal:  Neuroradiology       Date:  1995-11       Impact factor: 2.804

3.  PHACES association: a neuroradiologic review of 17 patients.

Authors:  V S Oza; E Wang; A Berenstein; M Waner; D Lefton; J Wells; F Blei
Journal:  AJNR Am J Neuroradiol       Date:  2008-01-25       Impact factor: 3.825

  3 in total

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