Kozak Igor, Mochida Ganeshwaran H, Lin Doris D M, Ali Syed M, Bosley Thomas M
Department of Ophthalmology and Vision Science, University of Arizona, Tucson, AZ, USA.
Research Department, Moorfields Eye Hospital Center, Abu Dhabi, United Arab Emirates.
Eye Brain. 2024 Oct 23;16:55-63. doi: 10.2147/EB.S419663. eCollection 2024.
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts (HDBSCC) is a rare syndrome caused by biallelic mutations in the JAM3 gene with significant intrafamilial variability in clinical presentation and brain imaging phenotypes. The clinical presentation of HDBSCC includes severe recurrent hemorrhages involving the brain parenchyma and the ventricles beginning in utero and continuing in infancy together with dense central cataracts present at birth. This comprehensive review documents reported cases on this unique condition and describes its genetic, neuroradiologic and ophthalmic features. It should be included in the differential diagnosis of children with congenital cataracts and neurodevelopmental abnormalities. Unique clinical, imaging findings and genetic testing can help the diagnosis.
脑内出血性破坏、室管膜下钙化和先天性白内障(HDBSCC)是一种罕见综合征,由JAM3基因的双等位基因突变引起,临床表现和脑成像表型在家族内具有显著变异性。HDBSCC的临床表现包括从子宫内开始并持续到婴儿期的累及脑实质和脑室的严重复发性出血,以及出生时即存在的致密中央性白内障。这篇综述记录了关于这种独特病症的报道病例,并描述了其遗传、神经放射学和眼科特征。它应纳入患有先天性白内障和神经发育异常儿童的鉴别诊断中。独特的临床、影像学表现及基因检测有助于诊断。