A novel FBN1 mutation in Marfan's syndrome with giant aortic root aneurysm.

Shi, J; Wang, J; Zhang, Y; Zhang, Y; Hou, Q; Zhang, L; Xie, M

Shi, J; Wang, J; Zhang, Y; Zhang, Y; Hou, Q; Zhang, L; Xie, M.

Afiliación

Shi J; Department of Ultrasound Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277# Jiefang Ave, Wuhan 430022, China.
Wang J; Clinical Research Center for Medical Imaging in Hubei Province, Wuhan 430022, China.
Zhang Y; Hubei Province Key Laboratory of Molecular Imaging, Wuhan 430022, China.
Zhang Y; Department of Ultrasound Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277# Jiefang Ave, Wuhan 430022, China.
Hou Q; Clinical Research Center for Medical Imaging in Hubei Province, Wuhan 430022, China.
Zhang L; Hubei Province Key Laboratory of Molecular Imaging, Wuhan 430022, China.
Xie M; Department of Ultrasound Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277# Jiefang Ave, Wuhan 430022, China.

QJM ; 117(7): 536-537, 2024 Jul 01.

Article en En | MEDLINE | ID: mdl-38532302

Asunto(s)

Fibrilina-1; Síndrome de Marfan; Mutación; Humanos; Síndrome de Marfan/genética; Síndrome de Marfan/complicaciones; Fibrilina-1/genética; Aneurisma de la Aorta/genética; Aneurisma de la Aorta/diagnóstico por imagen; Masculino; Adulto; Femenino; Aneurisma de la Raíz de la Aorta; Adipoquinas

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrilina-1 / Síndrome de Marfan / Mutación Límite: Adult / Female / Humans / Male Idioma: En Revista: QJM Asunto de la revista: MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: China

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