Genetic analysis of a family presenting with coexisting cerebral cavernous malformations and polycystic kidney disease

Genetic analysis of a family presenting with coexisting cerebral cavernous malformations and polycystic kidney disease

Hereditary cerebral cavernous malformations (CCMs) are characterized by clustered dilated capillary-like vessels in the brain. Autosomal dominant polycystic kidney disease (PKD) is characterized by renal cysts and extra-renal abnormalities. We report a Taiwanese family in which the index case exhibi...

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Bibliographic Details
Main Authors:	Pei-Feng Hsieh, Shih-Yao Liu, Chih-Hao Chen, Pei-Lung Chen, Sung-Chun Tang, Jiann-Shing Jeng
Format:	Article
Language:	English
Published:	Elsevier 2022-11-01
Series:	Journal of the Formosan Medical Association
Subjects:	CCM2 PKD2 Cerebral cavernous malformations Polycystic kidney disease
Online Access:	http://www.sciencedirect.com/science/article/pii/S0929664622001127

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