| Literature DB >> 24726473 |
Margaret J McMillin1, Anita E Beck2, Jessica X Chong1, Kathryn M Shively1, Kati J Buckingham1, Heidi I S Gildersleeve1, Mariana I Aracena3, Arthur S Aylsworth4, Pierre Bitoun5, John C Carey6, Carol L Clericuzio7, Yanick J Crow8, Cynthia J Curry9, Koenraad Devriendt10, David B Everman11, Alan Fryer12, Kate Gibson13, Maria Luisa Giovannucci Uzielli14, John M Graham15, Judith G Hall16, Jacqueline T Hecht17, Randall A Heidenreich7, Jane A Hurst18, Sarosh Irani19, Ingrid P C Krapels20, Jules G Leroy21, David Mowat22, Gordon T Plant23, Stephen P Robertson24, Elizabeth K Schorry25, Richard H Scott18, Laurie H Seaver26, Elliott Sherr27, Miranda Splitt28, Helen Stewart29, Constance Stumpel20, Sehime G Temel30, David D Weaver31, Margo Whiteford32, Marc S Williams33, Holly K Tabor34, Joshua D Smith35, Jay Shendure35, Deborah A Nickerson35, Michael J Bamshad36.
Abstract
Gordon syndrome (GS), or distal arthrogryposis type 3, is a rare, autosomal-dominant disorder characterized by cleft palate and congenital contractures of the hands and feet. Exome sequencing of five GS-affected families identified mutations in piezo-type mechanosensitive ion channel component 2 (PIEZO2) in each family. Sanger sequencing revealed PIEZO2 mutations in five of seven additional families studied (for a total of 10/12 [83%] individuals), and nine families had an identical c.8057G>A (p.Arg2686His) mutation. The phenotype of GS overlaps with distal arthrogryposis type 5 (DA5) and Marden-Walker syndrome (MWS). Using molecular inversion probes for targeted sequencing to screen PIEZO2, we found mutations in 24/29 (82%) DA5-affected families and one of two MWS-affected families. The presence of cleft palate was significantly associated with c.8057G>A (Fisher's exact test, adjusted p value < 0.0001). Collectively, although GS, DA5, and MWS have traditionally been considered separate disorders, our findings indicate that they are etiologically related and perhaps represent variable expressivity of the same condition.Entities:
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Year: 2014 PMID: 24726473 PMCID: PMC4067551 DOI: 10.1016/j.ajhg.2014.03.015
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025