Literature DB >> 14729417

Pyruvate dehydrogenase E1alpha subunit deficiency in a female patient: evidence of antenatal origin of brain damage and possible etiology of infantile spasms.

Naoko Wada1, Toyojiro Matsuishi, Michiko Nonaka, Etsuo Naito, Makoto Yoshino.   

Abstract

Enlargement of the lateral ventricles and atrophy of the brain were documented ultrasonographically in utero at as early as 28th week of gestation in a female patient with lactic acidosis due to deficiency of the pyruvate dehydrogenase E1alpha subunit, demonstrating that the changes characteristic of this disease can occur antenatally. The mechanism of infantile spasms in this disease may be linked to mosaicism of the brain cells involving the normal enzyme and the mutant enzyme.

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Year:  2004        PMID: 14729417     DOI: 10.1016/s0387-7604(03)00072-x

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  10 in total

Review 1.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2011-10-07       Impact factor: 4.797

2.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2012-07       Impact factor: 4.797

Review 3.  Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.

Authors:  Sophie Collardeau-Frachon; Marie-Pierre Cordier; Massimiliano Rossi; Laurent Guibaud; Christine Vianey-Saban
Journal:  J Inherit Metab Dis       Date:  2016-04-22       Impact factor: 4.982

4.  MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.

Authors:  Nicholas Ah Mew; Johanna B Loewenstein; Nadja Kadom; Uta Lichter-Konecki; Andrea L Gropman; Jodie M Martin; Adeline Vanderver
Journal:  Pediatr Neurol       Date:  2011-07       Impact factor: 3.372

5.  Nonspecific mitochondrial disease with epilepsy in children: diagnostic approaches and epileptic phenotypes.

Authors:  Hoon-Chul Kang; Ji Won Kwon; Young Mock Lee; Heung Dong Kim; Hong Jin Lee; Si Houn Hahn
Journal:  Childs Nerv Syst       Date:  2007-06-19       Impact factor: 1.475

Review 6.  In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.

Authors:  Erica B Sherry; Phil Lee; In-Young Choi
Journal:  Neurochem Res       Date:  2015-11-26       Impact factor: 3.996

7.  Neonatal pyruvate dehydrogenase deficiency due to a R302H mutation in the PDHA1 gene: MRI findings.

Authors:  João P Soares-Fernandes; Roseli Teixeira-Gomes; Romeu Cruz; Manuel Ribeiro; Zita Magalhães; Jaime F Rocha; Lara M Leijser
Journal:  Pediatr Radiol       Date:  2008-01-16

8.  Brain MR imaging and proton MR spectroscopy in female mice with pyruvate dehydrogenase complex deficiency.

Authors:  Lioudmila Pliss; Richard Mazurchuk; Joseph A Spernyak; Mulchand S Patel
Journal:  Neurochem Res       Date:  2007-03-07       Impact factor: 3.996

9.  Ketogenic diet in pyruvate dehydrogenase complex deficiency: short- and long-term outcomes.

Authors:  Kalliopi Sofou; Maria Dahlin; Tove Hallböök; Marie Lindefeldt; Gerd Viggedal; Niklas Darin
Journal:  J Inherit Metab Dis       Date:  2017-01-18       Impact factor: 4.982

Review 10.  Metabolic etiologies in West syndrome.

Authors:  Seda Salar; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia Open       Date:  2018-03-14
  10 in total

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