Literature DB >> 9028461

Dubowitz syndrome in a boy without developmental delay: further evidence for phenotypic variability.

R Wallerstein1, J Kacmar, C E Anderson, L Jackson.   

Abstract

Dubowitz syndrome is an autosomal recessive condition characterized by pre- and postnatal growth retardation, eczema, telecanthus, epicanthal folds, blepharophimosis, ptosis, and broadening of the bridge and tip of the nose. The initial patients described had varying degrees of mental retardation and there is little information about long-term developmental outcome. We present a boy with Dubowitz syndrome who does not have developmental delays, providing additional evidence that the phenotype includes normal neurodevelopmental status.

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Year:  1997        PMID: 9028461

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


  2 in total

1.  Endocrinological features of a patient with 14q microdeletion and Dubowitz phenotype.

Authors:  Maria Elisa Amodeo; Elena Inzaghi; Annalisa Deodati; Stefano Cianfarani
Journal:  Mol Genet Genomic Med       Date:  2021-03-31       Impact factor: 2.183

2.  Chromosome deletion of 14q32.33 detected by array comparative genomic hybridization in a patient with features of dubowitz syndrome.

Authors:  Diana C Darcy; Scott Rosenthal; Robert J Wallerstein
Journal:  Case Rep Genet       Date:  2011-09-28
  2 in total

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