Ullah Asmat, Gul Ajab, Umair Muhammad, Ahmad Farooq, Aziz Abdul, Wali Abdul, Ahmad Wasim
Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Department of Biotechnology and Informatics, BUITEMS, Quetta, Pakistan.
Genet Mol Biol. 2018 Jan-Mar;41(1):1-8. doi: 10.1590/1678-4685-GMB-2016-0162. Epub 2018 Jan 22.
Split-hand/split-foot malformation (SHFM), also known as ectrodactyly is a rare genetic disorder. It is a clinically and genetically heterogeneous group of limb malformations characterized by absence/hypoplasia and/or median cleft of hands and/or feet. To date, seven genes underlying SHFM have been identified. This study described four consanguineous families (A-D) segregating SHFM in an autosomal recessive manner. Linkage in the families was established to chromosome 12p11.1-q13.13 harboring WNT10B gene. Sequence analysis identified a novel homozygous nonsense variant (p.Gln154*) in exon 4 of the WNT10B gene in two families (A and B). In the other two families (C and D), a previously reported variant (c.300_306dupAGGGCGG; p.Leu103Argfs*53) was detected. This study further expands the spectrum of the sequence variants reported in the WNT10B gene, which result in the split hand/foot malformation.
裂手/裂足畸形(SHFM),也称为缺指(趾)畸形,是一种罕见的遗传性疾病。它是一组临床和遗传异质性的肢体畸形,其特征是手和/或脚的缺失/发育不全和/或正中裂。迄今为止,已鉴定出导致SHFM的七个基因。本研究描述了四个以常染色体隐性方式遗传SHFM的近亲家庭(A - D)。在家系中确定与含有WNT10B基因的12号染色体p11.1 - q13.13区域连锁。序列分析在两个家庭(A和B)的WNT10B基因外显子4中鉴定出一种新的纯合无义变异(p.Gln154*)。在另外两个家庭(C和D)中,检测到一个先前报道的变异(c.300_306dupAGGGCGG;p.Leu103Argfs*53)。本研究进一步扩展了WNT10B基因中报道的导致裂手/裂足畸形的序列变异谱。