Garavelli L, Leask K, Zanacca C, Pedori S, Albertini G, Della Giustina E, Croci G F, Magnani C, Banchini G, Clayton-Smith J, Bocian M, Firth H, Gold J A, Hurst J
Department of Paediatrics and Genetics Unit, S. Maria Nuova Hospital, Reggio Emilia, Italy.
Genet Couns. 2005;16(2):117-28.
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature: We describe the clinical history and magnetic resonance imaging (MRI) findings in 10 children with the Macrocephaly-Cutis Marmorata Telangiectatica Congenita syndrome (M-CMTC--MIM 602501). This syndrome has recently been delineated within the general group of patients with Cutis Marmorata Telangiectatica (CMTC) as a distinct and easily recognisable entity. In contrast to most children with CMTC, patients with M-CMTC syndrome have a high risk of neurological abnormalities, such as hydrocephalus, megalencephaly, developmental delay and mental retardation. An MRI scan showed structural cerebral abnormalities in all of our patients, including megalencephaly, asymmetry of the cerebral hemispheres and abnormally increased signal of white matter. Seven patients also had Chiari type I malformation. Reviewing all reported cases, we propose appropriate surveillance for known complications.
巨头畸形-先天性大理石样皮肤毛细血管扩张综合征的MRI及神经学表现:10例报告并文献复习:我们描述了10例巨头畸形-先天性大理石样皮肤毛细血管扩张综合征(M-CMTC--MIM 602501)患儿的临床病史及磁共振成像(MRI)表现。该综合征最近已在先天性大理石样皮肤毛细血管扩张症(CMTC)患者群体中被界定为一个独特且易于识别的实体。与大多数CMTC患儿不同,M-CMTC综合征患者存在神经学异常的高风险,如脑积水、巨脑症、发育迟缓及智力障碍。MRI扫描显示我们所有患者均存在脑结构异常,包括巨脑症、大脑半球不对称及白质信号异常增高。7例患者还患有Ⅰ型Chiari畸形。回顾所有已报道病例,我们建议对已知并发症进行适当监测。