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Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation

  • Published:2018-04-14 Issue:6 Volume:6 Page:1048-1050
  • ISSN:2050-0904
  • Container-title:Clinical Case Reports
  • language:en
  • Short-container-title:Clin Case Rep

Author:

Rosa Joana1ORCID,Fraga Ana Beatriz1,de Carvalho Rita2,Maia Ana Lúcia1,Rodrigues Ana Luísa1,Gomes Maria Fernanda1

Affiliation:

1. Pediatric Department; Hospital of Divino Espirito Santo of Ponta Delgada, EPER; São Miguel Island, Azores Portugal

2. Endocrinology and Nutrition Department; Hospital of Divino Espirito Santo of Ponta Delgada, EPER; São Miguel Island, Azores Portugal

Publisher

Wiley

Subject

General Medicine

Reference8 articles.

1. Methylmalonic and propionic acidemias: clinical management update;Fraser;Curr. Opin. Pediatr.,2016

2. Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia;Baumgartner;Orphanet. J. Rare Dis.,2014

3. Acrodermatitis dysmetabolica in an infant with maple syrup urine disease;Flores;Clin. Exp. Dermatol.,2016

4. Acrodermatitis enteropathica-like cutaneous lesions in organic aciduria;De Raeve;J. Pediatr.,1994

5. Consensus for the nutritional treatment of isovaleric, propionic and methylmalonic acidurias;Rocha;Acta. Pediatr. Port.,2008

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