Literature DB >> 16566017

Leigh's disease due to a new mutation in the PDHX gene.

Manuel Schiff1, Manuele Miné, Michèle Brivet, Cécile Marsac, Monique Elmaleh-Bergés, Philippe Evrard, Hélène Ogier de Baulny.   

Abstract

OBJECTIVE: To describe the clinical course, neuroradiological presentation, biochemical and molecular studies of a new patient with pyruvate dehydrogenase complex (PDHc) deficiency. To compare this case with the data on other published cases.
METHODS: Brain magnetic resonance imaging (MRI), basal metabolic investigations with lactate measurements in body fluids, PDHc activity assay on cultured skin fibroblasts, immunoblot analysis and molecular studies (polymerase chain reaction [PCR] and sequencing procedures).
RESULTS: Our patient accused an unspecific encephalopathy for years and presented at 13 years of age an acute deterioration with basal ganglia necrosis and subcortical white matter involvement. PDHc deficiency was secondary to a large deletion (3913 bp) in the PDHX gene, which encodes E3 binding protein (E3BP) subunit.
INTERPRETATION: These data provide an additional case of E3BP deficiency with a unique and previously unreported deletion in the PDHX gene.

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Year:  2006        PMID: 16566017     DOI: 10.1002/ana.20818

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  9 in total

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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
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Review 5.  Paroxysmal Movement Disorders: Recent Advances.

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6.  MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhood.

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Review 7.  The genetics of Leigh syndrome and its implications for clinical practice and risk management.

Authors:  Ilene S Ruhoy; Russell P Saneto
Journal:  Appl Clin Genet       Date:  2014-11-13

Review 8.  Molecular basis of Leigh syndrome: a current look.

Authors:  Manuela Schubert Baldo; Laura Vilarinho
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Authors:  May Yung Tiet; Zhiyuan Lin; Fei Gao; Matthew James Jennings; Rita Horvath
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  9 in total

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