Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA.
Clin Dysmorphol. 2020 Jul;29(3):127-131. doi: 10.1097/MCD.0000000000000327.
The clinical phenotype of 1q21.1 microdeletion syndrome is highly heterogeneous. It is characterized by dysmorphic facial features, microcephaly, and developmental delay. Several congenital defects, including cardiac, ocular, skeletal anomalies, and psychiatric or behavioural abnormalities, have also been described. Here, we report on two siblings with substantial intrafamilial phenotypic variability carrying a heterozygous deletion of the 1q21.1 region spanning a known critical genomic area (~1.35 Mb). The microdeletion was inherited from the unaffected father. Patients described here show a spectrum of clinical features, a portion of which overlap with those previously reported in patients with 1q21.1 microdeletions. In addition, we review the clinical reports of 66 individuals with this condition. These findings extend and substantiate the current clinical understanding of recurrent copy number variations in the 1q21.1 region.
1q21.1 微缺失综合征的临床表型高度异质。其特征为畸形面容、小头畸形和发育迟缓。也有一些先天性缺陷,包括心脏、眼部、骨骼异常以及精神或行为异常,已有描述。在此,我们报告了两例同胞患者,其携带 1q21.1 区域的杂合性缺失,该缺失跨越已知的关键基因组区域(约 1.35 Mb)。微缺失来自未受影响的父亲。本文所描述的患者表现出一系列的临床特征,其中一部分与先前报道的 1q21.1 微缺失患者的特征重叠。此外,我们还回顾了 66 例该病症患者的临床报告。这些发现扩展并证实了当前对 1q21.1 区域复发性拷贝数变异的临床认识。