5q14.3 Microdeletions: A Contiguous Gene Syndrome with Capillary Malformation-Arteriovenous Malformation Syndrome and Neurologic Findings

作者：Park Sung Min; Kim Jeong Min; Kim Gun Wook; Kim Hoon Soo; Kim Byung Soo; Kim Moon Bum; Ko Hyun Chang^*

来源：Pediatric Dermatology, 2017, 34(2): 156-159.

DOI：10.1111/pde.13088

Deletions within chromosome region 5q14.3q15 have been associated with a spectrum of disorders including developmental delay, hypotonia, absent speech, mild facial dysmorphism, seizures, and brain anomalies. Some cases of concomitant neurologic abnormalities and cutaneous vascular malformation associated with 5q14.3 deletion have been reported. Previously reported cases had similar features, including multiple capillary malformations, and neurologic abnormalities, including epilepsy, hypotonia, and developmental delay. We report a case of 5q14.3 neurocutaneous syndrome presenting with multiple capillary malformations, neurologic abnormalities, and microdeletion in chromosome 5q14.3.

• 出版日期2017-4