Literature DB >> 3137916

In utero central nervous system damage in pyruvate dehydrogenase deficiency.

K A Aleck1, A M Kaplan, W G Sherwood, B H Robinson.   

Abstract

Pyruvate dehydrogenase deficiency is among the most common causes of congenital lactic acidosis. We describe siblings with congenital lactic acidosis due to a deficiency of pyruvate dehydrogenase complex. The findings of computed tomography and pathologic studies suggest that central nervous system damage had occurred in utero. These observations have implications for treatment and outcome in patients with enzymatic defects causing congenital lactic acidosis.

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Year:  1988        PMID: 3137916     DOI: 10.1001/archneur.1988.00520330073012

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  3 in total

Review 1.  Magnetic resonance imaging in lactic acidosis.

Authors:  M S van der Knaap; C Jakobs; J Valk
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

2.  Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications.

Authors:  J F Samson; P G Barth; J I de Vries; F H Menko; W Ruitenbeek; B A van Oost; C Jakobs
Journal:  Eur J Pediatr       Date:  1994-07       Impact factor: 3.183

3.  Agenesis of the Corpus Callosum and Skeletal Deformities in Two Unrelated Patients: Analysis via MRI and Radiography.

Authors:  Ali Al Kaissi; Herbert Kurz; Wolfgang Bock; Gerald Pärtan; Klaus Klaushofer; Rudolf Ganger; Franz Grill
Journal:  Case Rep Orthop       Date:  2014-01-29
  3 in total

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