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• W2046895384 abstract "The popliteal pterygia syndromes are a distinct subset of the hundreds of Mendelian orofacial clefting syndromes. Popliteal pterygia syndromes have considerable variability in severity and in the associated phenotypic features but are all characterized by cutaneous webbing across one or more major joints, cleft lip and/or palate, syndactyly, and genital malformations. Heterozygous mutations in IRF6 cause popliteal pterygium syndrome (PPS) while homozygous mutations in RIPK4 or CHUK (IKKA) cause the more severe Bartsocas–Papas syndrome (BPS) and Cocoon syndrome, respectively. In this study, we report mutations in six pedigrees with children affected with PPS or BPS. Using a combination of Sanger and exome sequencing, we report the first case of an autosomal recessive popliteal pterygium syndrome caused by homozygous mutation of IRF6 and the first case of uniparental disomy of chromosome 21 leading to a recessive disorder. We also demonstrate that mutations in RIPK4 can cause features with a range of severity along the PPS‐BPS spectrum and that mutations in IKKA can cause a range of features along the BPS‐Cocoon spectrum. Our findings have clinical implications for genetic counseling of families with pterygia syndromes and further implicate IRF6 , RIPK4 , and CHUK ( IKKA ) in potentially interconnected pathways governing epidermal and craniofacial development. © 2015 Wiley Periodicals, Inc." @default.
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• W2046895384 date "2015-02-18" @default.
• W2046895384 modified "2023-10-16" @default.
• W2046895384 title "Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders" @default.
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• W2046895384 doi "https://doi.org/10.1002/ajmg.a.36896" @default.
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