Hospices Civils de Lyon, GHE, Service de Génétique, Lyon, France.
Laboratoire d'Environnement et de Santé, Université de Sidi Bel Abbés, UDL, Sidi Bel Abbés, Algeria.
Am J Med Genet A. 2024 Jul;194(7):e63580. doi: 10.1002/ajmg.a.63580. Epub 2024 Mar 21.
Deletions of the long arm of chromosome 20 (20q) are rare, with only 16 reported patients displaying a proximal interstitial 20q deletion. A 1.62 Mb minimal critical region at 20q11.2, encompassing three genes GDF5, EPB41L1, and SAMHD1, is proposed to be responsible for this syndrome. The leading clinical features include growth retardation, intractable feeding difficulties with gastroesophageal reflux, hypotonia and psychomotor developmental delay. Common facial dysmorphisms including triangular face, hypertelorism, and hypoplastic alae nasi were additionally reported. Here, we present the clinical and molecular findings of five new patients with proximal interstitial 20q deletions. We analyzed the phenotype and molecular data of all previously reported patients with 20q11.2q12 microdeletions, along with our five new cases. Copy number variation analysis of patients in our cohort has enabled us to identify the second critical region in the 20q11.2q12 region and redefine the first region that is initially identified. The first critical region spans 359 kb at 20q11.2, containing six MIM genes, including two disease-causing genes, GDF5 and CEP250. The second critical region spans 706 kb at 20q12, encompassing four MIM genes, including two disease-causing genes, MAFB and TOP1. We propose GDF5 to be the primary candidate gene generating the phenotype of patients with 20q11.2 deletions. Moreover, we hypothesize TOP1 as a potential candidate gene for the second critical region at 20q12. Of note, we cannot exclude the possibility of a synergistic role of other genes involved in the deletion, including a contiguous gene deletion syndrome or position effect affecting both critical regions. Further studies focusing on patients with proximal 20q deletions are required to support our hypothesis.
20 号染色体长臂缺失(20q)非常罕见,仅有 16 例患者表现为近端 20q 缺失[1,2]。20q11.2 上的 3 个基因(GDF5、EPB41L1 和 SAMHD1)组成的 1.62Mb 最小关键区域被认为与该综合征有关[3]。该综合征的主要临床特征包括生长迟缓、难以控制的胃食管反流喂养困难、低张力和精神运动发育迟缓[3]。还报道了常见的面部畸形,包括三角脸、远视和鼻翼发育不全[3]。在这里,我们介绍了 5 例近端 20q 缺失患者的临床和分子发现。我们分析了所有先前报道的 20q11.2q12 微缺失患者的表型和分子数据,以及我们的 5 例新病例。我们对本队列患者的拷贝数变异分析使我们能够识别 20q11.2q12 区域的第二个关键区域,并重新定义最初确定的第一个区域。第一个关键区域跨越 20q11.2 的 359kb,包含 6 个 MIM 基因,包括两个致病基因 GDF5 和 CEP250。第二个关键区域跨越 20q12 的 706kb,包含 4 个 MIM 基因,包括两个致病基因 MAFB 和 TOP1。我们提出 GDF5 是导致 20q11.2 缺失患者表型的主要候选基因。此外,我们假设 TOP1 是 20q12 第二个关键区域的潜在候选基因。需要注意的是,我们不能排除涉及缺失的其他基因的协同作用的可能性,包括连续基因缺失综合征或影响两个关键区域的位置效应。需要进一步研究近端 20q 缺失患者以支持我们的假设。