Whole-exome sequencing identifies a novel IHH insertion in an Ontario family with brachydactyly type A1. (December 2018)

• Record Type: Journal Article
• Authors: Ho, Rosettia; McIntyre, Adam D; Kennedy, Brooke A; Hegele, Robert A
• Is Part Of: SAGE open medical case reports. Volume 6(2018)
• Publication Date: 2018-12
• Subjects: Brachydactyly type A1 -- Indian hedgehog -- signalling molecule -- autosomal dominant disorder -- skeletal disorder -- whole-exome sequencing; Clinical medicine -- Case studies -- Periodicals; 616.09
• DOI: 10.1177/2050313X18818711
• Languages: English
• ISSNs: 2050-313X

Abstract

Isolated brachydactyly is an umbrella term describing disproportionally shortened fingers and toes, often following an autosomal dominant mode of inheritance. Various forms of brachydactyly have been characterized and several causative genes have been found, but many types remain genetically undefined. We describe an Ontario family with mild brachydactyly in which whole-exome sequencing identified a novel variant for brachydactyly type A1 (exon 1, c.285_287dupGAA, p.Glu95_Asn96insLys) in the Indian hedgehog ( IHH ) gene. This rare variant co-segregated with affected status in the pedigree and was associated with (1) shortened middle phalange length by 21.1% ( p < 0.001); (2) shortened palm length by 13.8% ( p < 0.01); (3) reduced digit-palm ratio by 6.8% ( p < 0.03); and (4) reduced stature by 9.5% ( p < 0.001). We report the first IHH in-frame insertion causing brachydactyly type A1.