Literature DB >> 15937946

A new observation of acro-cardio-facial syndrome substantiates interindividual clinical variability.

Rita Mingarelli1, Daniela Zuccarello, Maria Cristina Digilio, Bruno Dallapiccola.   

Abstract

We report on a baby presenting with ectrodactyly, heart defects, and mild facial dysmorphisms, an association recognized as acro-cardio-facial syndrome (ACFS). Based on the first three observations, the acronym CCGE, cleft palate, cardiac defect, genital anomalies, and ectrodactyly had been proposed to embrace the most consistent features of this syndrome. A subsequent report and the present patient point to an obvious interindividual and intrafamilial variability of this autosomal recessive disorder in which ectrodactyly was the sole characteristic shared by all affected individuals. Copyright (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15937946     DOI: 10.1002/ajmg.a.30770

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Confirmation of 6q21-6q22.1 deletion in acro-cardio-facial syndrome and further delineation of this contiguous gene deletion syndrome.

Authors:  Cindy Hudson; Corbin Schwanke; John P Johnson; Abdallah F Elias; Sandy Phillips; Tammy Schwalbe; Mary Tunby; Dongbin Xu
Journal:  Am J Med Genet A       Date:  2014-04-08       Impact factor: 2.802

Review 2.  Acro-cardio-facial syndrome.

Authors:  Maria Cristina Digilio; Bruno Dallapiccola
Journal:  Orphanet J Rare Dis       Date:  2010-09-29       Impact factor: 4.123

  2 in total

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