Prenatal presentation of hereditary hemorrhagic telangiectasia - a report of two sibs.

Saleh, Maha; Miron, Ioana; Al-Rukban, Hadeel; Chitayat, David; Nezarati, Marjan M

Saleh, Maha; Miron, Ioana; Al-Rukban, Hadeel; Chitayat, David; Nezarati, Marjan M.

Afiliação

Saleh M; The Prenatal Diagnosis, Medical Genetics Program, Department of Obstetrics, Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.
Miron I; Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, Toronto, ON, Canada.
Al-Rukban H; The Prenatal Diagnosis, Medical Genetics Program, Department of Obstetrics, Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.
Chitayat D; Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, Toronto, ON, Canada.
Nezarati MM; The Prenatal Diagnosis, Medical Genetics Program, Department of Obstetrics, Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.

Prenat Diagn ; 36(9): 891-3, 2016 Sep.

Article em En | MEDLINE | ID: mdl-27381467

Assuntos

Receptores de Activinas Tipo II/genética; Malformações Arteriovenosas/genética; Hepatopatias/genética; Telangiectasia Hemorrágica Hereditária/diagnóstico; Feminino; Humanos; Recém-Nascido; Hepatopatias/congênito; Masculino; Gravidez; Telangiectasia Hemorrágica Hereditária/genética; Ultrassonografia Pré-Natal

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Telangiectasia Hemorrágica Hereditária / Receptores de Activinas Tipo II / Hepatopatias Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male / Newborn / Pregnancy Idioma: En Revista: Prenat Diagn Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google