Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria

Abstract Background Cobalamin metabolism disorders are rare, inherited diseases which cause megaloblastic anaemia and other clinical manifestations. Early diagnosis of these conditions is essential, in order to allow appropriate treatment as early as possible. Case presentation Here we report the ca...

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Bibliographic Details
Main Authors: Elvira Grandone, Pasquale Martinelli, Michela Villani, Gennaro Vecchione, Lucia Fischetti, Angelica Leccese, Rosa Santacroce, Gaetano Corso, Maurizio Margaglione
Format: Article
Language:English
Published: BMC 2019-08-01
Series:BMC Pregnancy and Childbirth
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12884-019-2474-5