Tucci Arianna, Pezzani Lidia, Scuvera Giulietta, Ronzoni Luisa, Scola Elisa, Esposito Susanna, Milani Donatella
Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.
Division of Neuroradiology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Am J Med Genet A. 2017 Mar;173(3):638-646. doi: 10.1002/ajmg.a.38054. Epub 2016 Dec 25.
Cutis Verticis Gyrata-Intellectual Disability (CVG-ID) syndrome is a rare neurocutaneous syndrome characterized by intellectual disability and scalp folds and furrows that are typically absent at birth and are first noticed after puberty. First reported in 1893, the syndrome was mainly identified in subjects living in psychiatric institutions, where it was found to have a prevalence of up to 11.4%. Most patients were reported in the literature during the first half of the 20th century. CVG-ID is now a less reported and possibly under-recognized syndrome. Here, we report a patient with CVG-ID that was diagnosed using the novel approach of magnetic resonance imaging and we conduct a systematic review of all patients reported in the last 60 years, discussing the core clinical features of this syndrome. © 2016 Wiley Periodicals, Inc.
头皮回状-智力障碍(CVG-ID)综合征是一种罕见的神经皮肤综合征,其特征为智力障碍以及头皮褶皱,这些褶皱在出生时通常并不存在,而是在青春期后首次被注意到。该综合征于1893年首次报道,主要在居住于精神病院的患者中被识别,在那里发现其患病率高达11.4%。20世纪上半叶,文献中报道了大多数患者。CVG-ID现在是一种报道较少且可能未被充分认识的综合征。在此,我们报告一名通过磁共振成像新方法诊断的CVG-ID患者,并对过去60年报道的所有患者进行系统综述,讨论该综合征的核心临床特征。© 2016威利期刊公司