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GNAQ 和 SLC26A4 基因突变引起的大前庭水管综合征相关的葡萄酒色斑:病例报告。

Port-wine stains associated with large vestibular aqueduct syndrome caused by mutations in GNAQ and SLC26A4 genes: A case report.

机构信息

Department of Dermatology, West China Hospital, Sichuan University, Chengdu, China.

出版信息

J Dermatol. 2020 Jan;47(1):78-81. doi: 10.1111/1346-8138.15130. Epub 2019 Nov 6.

Abstract

Port-wine stains (PWS) are capillary malformations associated with mutation in the GNAQ (NM_000441.1) gene. Large vestibular aqueduct syndrome (LVAS), caused by mutation in the SLC26A4 (NM_002072) gene, is an inner ear malformation that can lead to hearing loss. To our knowledge, LVAS in PWS patients has never been reported. Here, we describe a case of a 9-year-old female patient diagnosed with PWS on the face and neck, coexisting with large vestibular aqueduct syndrome. Further analyses revealed a somatic mutation in GNAQ and a compound heterozygous mutation in the SLC26A4 gene. Some PWS patients have associated abnormalities, such as glaucoma and choroidal hemangioma, leptomeningeal angiomas and atrophy or hypertrophy of bone and soft tissue. We present here the first case that reveals the possibility that capillary malformations are associated with inner ear malformation. More case reports and further studies are needed to determine whether these conditions coexist in other patients.

摘要

葡萄酒色斑(PWS)是与 GNAQ(NM_000441.1)基因突变相关的毛细血管畸形。大前庭水管综合征(LVAS)是由 SLC26A4(NM_002072)基因突变引起的内耳畸形,可导致听力损失。据我们所知,PWS 患者的 LVAS 从未有过报道。在此,我们描述了一例 9 岁女性患者,其面部和颈部患有葡萄酒色斑,同时伴有大前庭水管综合征。进一步分析显示 GNAQ 存在体细胞突变,SLC26A4 基因存在复合杂合突变。一些 PWS 患者存在相关的异常,如青光眼和脉络膜血管瘤、软脑膜血管畸形以及骨骼和软组织的萎缩或肥大。我们在此首次提出了毛细血管畸形与内耳畸形相关的可能性。需要更多的病例报告和进一步的研究来确定这些情况是否在其他患者中同时存在。

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