Raine syndrome: Report of a novel mutation and review of the different antenatal imaging modalities used to diagnose this disease.

Rameh, Georges; Megarbane, Andre; Jalbout, Liliane; Snaifer, Elie; Saliba, Souha; Nassar, Anwar; Chalouhi, Gihad

Rameh, Georges; Megarbane, Andre; Jalbout, Liliane; Snaifer, Elie; Saliba, Souha; Nassar, Anwar; Chalouhi, Gihad.

Afiliação

Rameh G; Department of Obstetrics and Gynecology, American University of Beirut Medical Center, Beirut, Lebanon.
Megarbane A; Department of Human Genetics, Lebanese American University Medical Center, Beirut, Lebanon.
Jalbout L; Department of Obstetrics and Gynecology, Mount Lebanon Hospital, Beirut, Lebanon.
Snaifer E; Department of Obstetrics and Gynecology, Saint Georges Hospital, Beirut, Lebanon.
Saliba S; Department of Radiology, Hotel Dieu de France, Beirut, Lebanon.
Nassar A; Department of Obstetrics and Gynecology, American University of Beirut Medical Center, Beirut, Lebanon.
Chalouhi G; Department of Obstetrics and Gynecology, American University of Beirut Medical Center, Beirut, Lebanon.

Prenat Diagn ; 42(5): 589-600, 2022 05.

Article em En | MEDLINE | ID: mdl-35373843

Assuntos

Calcinose; Exoftalmia; Morte Perinatal; Anormalidades Múltiplas; Caseína Quinase I/genética; Fissura Palatina; Proteínas da Matriz Extracelular/genética; Feminino; Humanos; Recém-Nascido; Microcefalia; Mutação; Osteosclerose; Gravidez

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Calcinose / Exoftalmia / Morte Perinatal Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Prenat Diagn Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Líbano

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