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Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?
Léticée, Nadia; Bessières-Grattagliano, Bettina; Dupré, Thierry; Vuillaumier-Barrot, Sandrine; de Lonlay, Pascale; Razavi, Ferechté; El Khartoufi, Nadia; Ville, Yves; Vekemans, Michel; Bouvier, Raymonde; Seta, Nathalie; Attié-Bitach, Tania.
Affiliation
  • Léticée N; AP-HP, Hôpital Necker-Enfants Malades, Centre de médecine fœtale et Maternité de Necker-Brune, Paris, France.
Mol Genet Metab ; 101(2-3): 253-7, 2010.
Article in En | MEDLINE | ID: mdl-20638314
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Full text: 1 Database: MEDLINE Main subject: Hydrops Fetalis / Phosphotransferases (Phosphomutases) Type of study: Diagnostic_studies / Etiology_studies / Systematic_reviews Limits: Female / Humans / Pregnancy Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2010 Type: Article Affiliation country: France
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Full text: 1 Database: MEDLINE Main subject: Hydrops Fetalis / Phosphotransferases (Phosphomutases) Type of study: Diagnostic_studies / Etiology_studies / Systematic_reviews Limits: Female / Humans / Pregnancy Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2010 Type: Article Affiliation country: France