Literature DB >> 561341

Hereditary nonprogressive athetotic hemiplegia: a new syndrome.

F Haar, P Dyken.   

Abstract

A family with four affected members showed a stereotyped unilateral neurologic deficit. The disorder was characterized in each member by congenital left hemiparesis, with subsequent development of left hemihypoplasia and athetoid posturing of the left hand. Although the proband was initially considered a "cerebral palsy" victim, the autosomal dominant pattern and the stereotyped clinical features in all affected family members suggest a hereditary process. Hereditary factors may be an uncommon cause of static unilateral neurologic motor defects.

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Year:  1977        PMID: 561341     DOI: 10.1212/wnl.27.9.849

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  2 in total

1.  Familial porencephaly.

Authors:  N J Shastri; S A Bharani; U J Modi; C Trivedi
Journal:  Indian J Pediatr       Date:  1993 May-Jun       Impact factor: 1.967

2.  Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly.

Authors:  G Breedveld; I F de Coo; M H Lequin; W F M Arts; P Heutink; D B Gould; S W M John; B Oostra; G M S Mancini
Journal:  J Med Genet       Date:  2005-08-17       Impact factor: 6.318

  2 in total

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