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[Proceedings: Infantile cerebral poliodystrophy (Alper's disease) in an infant with hyperlactacidemia and hepatic pyruvate carboxylase].

AuthorsM David, P Baltassat, B Dinjon, B Lauras, R De Villard, M Tommasi, J Gilly
JournalArchives francaises de pediatrie (Arch Fr Pediatr) 1975 Jun-Jul Vol. 32 Issue 6 Pg. 580 ISSN: 0003-9764 [Print] France
Vernacular TitlePoliodystrophie cérébrale infantile (maladie d'Alpers) chez un nourrisson avec hyperlactacidémie et anomalie de la pyruvate carboxylase hépatique
PMID1180638 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Lactates
  • Pyruvate Carboxylase
Topics
  • Ataxia (diagnosis)
  • Cerebral Cortex (pathology)
  • Child, Preschool
  • Diffuse Cerebral Sclerosis of Schilder (diagnosis)
  • Female
  • Humans
  • Infant
  • Lactates (blood)
  • Liver (enzymology)
  • Myoclonus (diagnosis)
  • Pyruvate Carboxylase (metabolism)
  • Syndrome

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