Literature DB >> 10482880

Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect.

Y C Hsieh1, J W Hou.   

Abstract

We report on a boy with pseudo-cleft of the upper lip, cleft palate, bifid uvula, lobulated tongue, hypoplasia of the epiglottis, both preaxial and central polydactyly of the hands (Y-shaped fourth metacarpals), bilateral preaxial polydactyly of the feet, postaxial polydactyly of the left foot, hearing impairment, and congenital heart disease with endocardial cushion defect. These clinical manifestations resembled oral-facial-digital syndrome type II (OFDS II, Mohr syndrome) or type VI (Váradi syndrome), associated with an atrioventricular canal. Clinical variability of OFDS II has been observed repeatedly. To the best of our knowledge, this is the first reported case of OFDS II with Y-shaped fourth metacarpals. In addition to Y-shaped fourth metacarpals, Mohr syndrome plus atrioventricular canal and hypoplasia of the epiglottis may represent an additional subgroup of OFDS. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10482880

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


  5 in total

1.  Laryngeal and tracheal anomalies in an infant with oral-facial-digital syndrome type VI (Váradi-Papp): report of a transitional type.

Authors:  Laura L Hayes; Stephen F Simoneaux; Susan Palasis; Dmitriy M Niyazov
Journal:  Pediatr Radiol       Date:  2008-05-14

2.  The many faces of oral-facial-digital syndrome.

Authors:  E Sukarova-Angelovska; N Angelkova; S Palcevska-Kocevska; M Kocova
Journal:  Balkan J Med Genet       Date:  2012-06       Impact factor: 0.519

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Authors:  Michinori Toriyama; Chanjae Lee; S Paige Taylor; Ivan Duran; Daniel H Cohn; Ange-Line Bruel; Jacqueline M Tabler; Kevin Drew; Marcus R Kelly; Sukyoung Kim; Tae Joo Park; Daniela A Braun; Ghislaine Pierquin; Armand Biver; Kerstin Wagner; Anne Malfroot; Inusha Panigrahi; Brunella Franco; Hadeel Adel Al-Lami; Yvonne Yeung; Yeon Ja Choi; Yannis Duffourd; Laurence Faivre; Jean-Baptiste Rivière; Jiang Chen; Karen J Liu; Edward M Marcotte; Friedhelm Hildebrandt; Christel Thauvin-Robinet; Deborah Krakow; Peter K Jackson; John B Wallingford
Journal:  Nat Genet       Date:  2016-05-09       Impact factor: 38.330

4.  Tbx2 terminates shh/fgf signaling in the developing mouse limb bud by direct repression of gremlin1.

Authors:  Henner F Farin; Timo H-W Lüdtke; Martina K Schmidt; Susann Placzko; Karin Schuster-Gossler; Marianne Petry; Vincent M Christoffels; Andreas Kispert
Journal:  PLoS Genet       Date:  2013-04-25       Impact factor: 5.917

5.  Distinctive Skeletal Abnormalities With No Microdeletions or Microduplications on Array-CGH in a Boy With Mohr Syndrome (Oro-Facial-Digital Type II).

Authors:  Ali Al Kaissi; Renata Pospischill; Franz Grill; Rudolf Ganger
Journal:  J Clin Med Res       Date:  2015-10-23
  5 in total

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