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[Latest advances in the diagnosis and treatment of Marfan syndrome]. / 马方综合征的最新诊疗进展.
Yang, Shu-Ting; Luo, Fang.
  • Yang ST; Department of Pediatrics, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 311100, China.
  • Luo F; Department of Pediatrics, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 311100, China.
Zhongguo Dang Dai Er Ke Za Zhi ; 24(7): 826-831, 2022 Jul 15.
Article en Zh | MEDLINE | ID: mdl-35894201
ABSTRACT
Marfan syndrome (MFS) is a multisystem connective tissue disease with autosomal dominant inheritance. It is mainly caused by FBN1 gene mutation and often has different clinical manifestations. Neonatal MFS is especially rare with severe conditions and a poor prognosis. At present, there is still no radical treatment method for MFS, but early identification, early diagnosis, and early treatment can effectively prolong the life span of patients. This article reviews the latest advances in the diagnosis and treatment of MFS.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Marfan Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans / Newborn Idioma: Zh Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Marfan Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans / Newborn Idioma: Zh Año: 2022 Tipo del documento: Article