Literature DB >> 9208417

Moyamoya disease in a child with glycogen storage disease type Ia.

F Goutières1, M Bourgeois, P Trioche, J F Demelier, M Odievre, P Labrune.   

Abstract

A three-year-old child affected by glycogen storage disease (GSD) type Ia presented with acute hemiplegia secondary to Moyamoya disease. So far, the association of moyamoya with GSD Ia had only been reported twice. The rarity of both conditions makes their association unlikely to be a chance event and an etiological relationship between them must be considered.

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Year:  1997        PMID: 9208417     DOI: 10.1055/s-2007-973688

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  3 in total

1.  Perioperative management of hemostasis for surgery of benign hepatic adenomas in patients with glycogen storage disease type ia.

Authors:  Alix Mollet-Boudjemline; Aurélie Hubert-Buron; Catherine Boyer-Neumann; Roxana Aldea; Dominique Franco; Pascale Trioche-Eberschweiller; Anne-Elisabeth Mas; Mylène Mabille; Philippe Labrune; Vincent Gajdos
Journal:  JIMD Rep       Date:  2011-06-22

2.  Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type Ia.

Authors:  P Trioche; J Francoual; L Capel; M Odièvre; A Lindenbaum; P Labrune
Journal:  J Inherit Metab Dis       Date:  2000-03       Impact factor: 4.982

3.  Moyamoya and progressive myoclonic epilepsy secondary to CLN6 bi-allelic mutations - A previously unreported association.

Authors:  Jamie Talbot; Priyanka Singh; Clinda Puvirajasinghe; Sanjay M Sisodiya; Fergus Rugg-Gunn
Journal:  Epilepsy Behav Rep       Date:  2020-08-31
  3 in total

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