Literature DB >> 11102932

Uruguay facio-cardio-musculo-skeletal syndrome: a novel X-linked recessive disorder.

R Quadrelli1, A Vaglio, S Reyno, A Lemes, D Salazar, R S Lachman, W R Wilcox.   

Abstract

We report on three male patients from a single family with a brachyturricephaly, "pugilistic" facial appearance, a muffled voice, cardiomyopathy, muscular hypertrophy, broad hands, wide feet with progressive pes cavus deformities, dislocation of toes, variable congenital hip dislocation, and scoliosis. Three other males in the family, now deceased from cardiac disease, appear to have had the same disorder. The mother of the propositus has milder signs of the syndrome. All affected males are related through the maternal line. These cases represent an apparently previously undescribed X-linked recessive syndrome.

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Year:  2000        PMID: 11102932     DOI: 10.1002/1096-8628(20001127)95:3<247::aid-ajmg12>3.0.co;2-2

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac Death.

Authors:  Yuan Xue; Benedikt Schoser; Aliz R Rao; Roberto Quadrelli; Alicia Vaglio; Verena Rupp; Christine Beichler; Stanley F Nelson; Gudrun Schapacher-Tilp; Christian Windpassinger; William R Wilcox
Journal:  Circ Cardiovasc Genet       Date:  2016-03-01
  1 in total

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