Literature DB >> 8917246

Primary treatment of propionic acidemia complicated by acute thiamine deficiency.

D Matern1, H H Seydewitz, W Lehnert, H Niederhoff, J U Leititis, M Brandis.   

Abstract

Propionic acidemia is often manifested during the neonatal period with vomiting, failure to thrive, lethargy, and hyperammonemic coma when catabolism is prolonged. Mild lactic acidosis frequently accompanies metabolic decompensation. We present two patients with propionic acidemia whose initial manifestation was complicated by severe lactic acidosis caused by thiamine deficiency, which resulted from an inadequate supply of, and an increased need for, thiamine during metabolic stress. To prevent acute thiamine deficiency, we propose early vitamin supplementation during treatment of any severe metabolic decompensation accompanied by insufficient food intake.

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Year:  1996        PMID: 8917246     DOI: 10.1016/s0022-3476(96)70162-2

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  8 in total

1.  Metabolic decompensation and lactic acidosis in propionic acidaemia complicated by thiamine deficiency.

Authors:  E Mayatepek; A Schulze
Journal:  J Inherit Metab Dis       Date:  1999-04       Impact factor: 4.982

Review 2.  Nutrition therapy of organic acidaemias with amino acid-based formulas: emphasis on methylmalonic and propionic acidaemia.

Authors:  Steven Yannicelli
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

3.  Wernicke-like encephalopathy during classic maple syrup urine disease decompensation.

Authors:  R Manara; M Del Rizzo; A P Burlina; A Bordugo; V Citton; P Rodriguez-Pombo; M Ugarte; A B Burlina
Journal:  J Inherit Metab Dis       Date:  2012-02-18       Impact factor: 4.982

Review 4.  Patterns of brain injury in inborn errors of metabolism.

Authors:  Andrea L Gropman
Journal:  Semin Pediatr Neurol       Date:  2012-12       Impact factor: 1.636

Review 5.  Methylmalonic and propionic acidemias: clinical management update.

Authors:  Jamie L Fraser; Charles P Venditti
Journal:  Curr Opin Pediatr       Date:  2016-12       Impact factor: 2.856

6.  Extracorporeal membrane oxygenation in a patient with propionic acidaemia: a therapeutic option for cardiac failure.

Authors:  K Mizuguchi; H Hoshino; T Nagasawa; M Kubota
Journal:  J Inherit Metab Dis       Date:  2009-05-04       Impact factor: 4.982

Review 7.  Emergency management of inherited metabolic diseases.

Authors:  V Prietsch; M Lindner; J Zschocke; W L Nyhan; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2002-11       Impact factor: 4.982

Review 8.  Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia.

Authors:  Matthias R Baumgartner; Friederike Hörster; Carlo Dionisi-Vici; Goknur Haliloglu; Daniela Karall; Kimberly A Chapman; Martina Huemer; Michel Hochuli; Murielle Assoun; Diana Ballhausen; Alberto Burlina; Brian Fowler; Sarah C Grünert; Stephanie Grünewald; Tomas Honzik; Begoña Merinero; Celia Pérez-Cerdá; Sabine Scholl-Bürgi; Flemming Skovby; Frits Wijburg; Anita MacDonald; Diego Martinelli; Jörn Oliver Sass; Vassili Valayannopoulos; Anupam Chakrapani
Journal:  Orphanet J Rare Dis       Date:  2014-09-02       Impact factor: 4.123

  8 in total

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