Mohammed Idris, Al-Khawaga Sara, Bohanna David, Shabani Abdusamea, Khan Faiyaz, Love Donald R, Nawaz Zafar, Hussain Khalid
College of Health & Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.
Division of Endocrinology, Department of Pediatric Medicine, Sidra Medicine, Doha, Qatar.
Mol Genet Genomic Med. 2020 Jun;8(6):e1086. doi: 10.1002/mgg3.1086. Epub 2020 Apr 11.
There are few reports describing the proximal deletions of the short arm of chromosome 20, making it difficult to predict the likely consequences of these deletions. Most previously reported cases have described the association of 20p11.2 deletions with Alagille syndrome, while there are others that include phenotypes such as panhypopituitarism, craniofacial dysmorphism, polysplenia, autism, and Hirschsprung disease.
Molecular karyotyping, cytogenetics, and DNA sequencing were undertaken in a child to study the genetic basis of a complex phenotype consisting of craniofacial dysmorphism, ocular abnormalities, ectopic inguinal testes, polysplenia, growth hormone deficiency, central hypothyroidism, and gastrointestinal system anomalies.
We report the smallest described de novo proximal 20p11.2 deletion, which deletes only the FOXA2 leading to the above complex phenotype.
Haploinsufficiency of the FOXA2 only gene is associated with a multisystem disorder.
关于20号染色体短臂近端缺失的报道较少,因此很难预测这些缺失可能产生的后果。大多数先前报道的病例描述了20p11.2缺失与阿拉吉列综合征的关联,而其他病例则包括全垂体功能减退、颅面畸形、多脾症、自闭症和先天性巨结肠等表型。
对一名儿童进行了分子核型分析、细胞遗传学和DNA测序,以研究由颅面畸形、眼部异常、腹股沟异位睾丸、多脾症、生长激素缺乏、中枢性甲状腺功能减退和胃肠系统异常组成的复杂表型的遗传基础。
我们报告了所描述的最小的新发近端20p11.2缺失,该缺失仅删除了FOXA2基因,导致了上述复杂表型。
FOXA2单基因的单倍剂量不足与一种多系统疾病相关。