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SHANK3 相关的佩兰-麦克德米德综合征的定义和临床变异性。

Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome.

机构信息

Institute for Anatomy and Cell Biology, Ulm University, Ulm, Germany.

Instituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, ISCIII; ITHACA-European Reference Network, Hospital La Paz, Madrid, Spain.

出版信息

Eur J Med Genet. 2023 Jul;66(7):104754. doi: 10.1016/j.ejmg.2023.104754. Epub 2023 Mar 31.

Abstract

Phelan-McDermid syndrome (PMS) is an infrequently described syndrome that presents with a disturbed development, neurological and psychiatric characteristics, and sometimes other comorbidities. As part of the development of European medical guidelines we studied the definition, phenotype, genotype-phenotype characteristics, and natural history of the syndrome. The number of confirmed diagnoses of PMS in different European countries was also assessed and it could be concluded that PMS is underdiagnosed. The incidence of PMS in European countries is estimated to be at least 1 in 30,000. Next generation sequencing, including analysis of copy number variations, as first tier in diagnostics of individuals with intellectual disability will likely yield a larger number of individuals with PMS than presently known. A definition of PMS by its phenotype is at the present not possible, and therefore PMS-SHANK3 related is defined by the presence of SHANK3 haploinsufficiency, either by a deletion involving region 22q13.2-33 or a pathogenic/likely pathogenic variant in SHANK3. In summarizing the phenotype, we subdivided it into that of individuals with a 22q13 deletion and that of those with a pathogenic/likely pathogenic SHANK3 variant. The phenotype of individuals with PMS is variable, depending in part on the deletion size or whether only a variant of SHANK3 is present. The core phenotype in the domains development, neurology, and senses are similar in those with deletions and SHANK3 variants, but individuals with a SHANK3 variant more often are reported to have behavioural disorders and less often urogenital malformations and lymphedema. The behavioural disorders may, however, be a less outstanding feature in individuals with deletions accompanied by more severe intellectual disability. Data available on the natural history are limited. Results of clinical trials using IGF-1, intranasal insulin, and oxytocin are available, other trials are in progress. The present guidelines for PMS aim at offering tools to caregivers and families to provide optimal care to individuals with PMS.

摘要

佩兰-麦克德米德综合征(PMS)是一种罕见的综合征,表现为发育障碍、神经和精神特征,有时还有其他合并症。作为制定欧洲医学指南的一部分,我们研究了该综合征的定义、表型、基因型-表型特征和自然史。还评估了不同欧洲国家确诊的 PMS 病例数,可以得出结论,PMS 被低估了。估计欧洲国家的 PMS 发病率至少为每 30,000 人中有 1 例。下一代测序,包括拷贝数变异分析,作为诊断智力障碍个体的一线方法,可能会发现比目前已知更多的 PMS 患者。目前,由于 PMS 的表型无法定义,因此将 PMS-SHANK3 相关定义为 SHANK3 杂合性缺失,缺失区域包括 22q13.2-33 或 SHANK3 中的致病性/可能致病性变异。在总结表型时,我们将其分为存在 22q13 缺失的个体和存在致病性/可能致病性 SHANK3 变异的个体。PMS 患者的表型存在差异,部分取决于缺失大小或是否仅存在 SHANK3 变异。具有 PMS 的个体在发育、神经和感觉等领域的核心表型在缺失和 SHANK3 变异患者中相似,但存在 SHANK3 变异的个体更常报告存在行为障碍,而较少出现泌尿生殖畸形和淋巴水肿。然而,在伴有更严重智力障碍的缺失患者中,行为障碍可能不是一个突出的特征。目前可获得的自然史数据有限。已获得使用 IGF-1、鼻内胰岛素和催产素的临床试验结果,其他试验正在进行中。本 PMS 指南旨在为护理人员和家庭提供工具,为 PMS 患者提供最佳护理。

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