Mannose phosphate isomerase deficiency-congenital disorder of glycosylation (MPI-CDG) with cerebral venous sinus thrombosis as first and only presenting symptom: A rare but treatable cause of thrombophilia.

Mühlhausen, Chris; Henneke, Lisa; Schlotawa, Lars; Behme, Daniel; Grüneberg, Marianne; Gärtner, Jutta; Marquardt, Thorsten

Mühlhausen, Chris; Henneke, Lisa; Schlotawa, Lars; Behme, Daniel; Grüneberg, Marianne; Gärtner, Jutta; Marquardt, Thorsten.

Afiliação

Mühlhausen C; Department of Pediatrics and Adolescent Medicine University Medical Centre Göttingen Göttingen Germany.
Henneke L; Department of Pediatrics and Adolescent Medicine University Medical Centre Göttingen Göttingen Germany.
Schlotawa L; Department of Pediatrics and Adolescent Medicine University Medical Centre Göttingen Göttingen Germany.
Behme D; Department of Neuroradiology University Medical Centre Göttingen Göttingen Germany.
Grüneberg M; Department of General Paediatrics University of Münster Münster Germany.
Gärtner J; Department of Pediatrics and Adolescent Medicine University Medical Centre Göttingen Göttingen Germany.
Marquardt T; Department of General Paediatrics University of Münster Münster Germany.

JIMD Rep ; 55(1): 38-43, 2020 Sep.

Article em En | MEDLINE | ID: mdl-32905087

Palavras-chave

MPICDG; antithrombin deficiency; cerebral venous sinus thrombosis; coagulation disorder; congenital disorder of glycosylation; thrombophilia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: JIMD Rep Ano de publicação: 2020 Tipo de documento: Article

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