Intracranial Hemorrhage as the First Manifestation of Severe Congenital Factor X Deficiency in a 20-Month-Old Male: Case Report and Review of the Literature.

Diesch, Tamara; von der Weid, Nicolas Xavier; Schifferli, Alexandra; Kühne, Thomas

Diesch, Tamara; von der Weid, Nicolas Xavier; Schifferli, Alexandra; Kühne, Thomas.

Afiliación

Diesch T; Division of Paediatric Oncology/Haematology, University Children's Hospital Basel, Basel, Switzerland.
von der Weid NX; Division of Paediatric Oncology/Haematology, University Children's Hospital Basel, Basel, Switzerland.
Schifferli A; Division of Paediatric Oncology/Haematology, University Children's Hospital Basel, Basel, Switzerland.
Kühne T; Division of Paediatric Oncology/Haematology, University Children's Hospital Basel, Basel, Switzerland.

Pediatr Blood Cancer ; 63(7): 1300-4, 2016 07.

Article en En | MEDLINE | ID: mdl-27098186

Asunto(s)

Deficiencia del Factor X; Factor X/administración & dosificación; Hemorragias Intracraneales; Deficiencia del Factor X/complicaciones; Deficiencia del Factor X/diagnóstico; Deficiencia del Factor X/tratamiento farmacológico; Deficiencia del Factor X/patología; Humanos; Lactante; Hemorragias Intracraneales/diagnóstico; Hemorragias Intracraneales/etiología; Hemorragias Intracraneales/patología; Hemorragias Intracraneales/prevención & control; Masculino

Palabras clave

FX deficiency; bleeding tendency; missense mutation; prophylaxis; replacement therapy

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factor X / Hemorragias Intracraneales / Deficiencia del Factor X Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans / Infant / Male Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2016 Tipo del documento: Article País de afiliación: Suiza

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