Literature DB >> 1793348

[Dubowitz syndrome. A diagnosis not to be missed].

M Mathieu1, P Berquin, S Epelbaum, C Lenaerts, C Piussan.   

Abstract

Dubowitz syndrome is a rare hereditary disorder whose main features are intra-uterine and post-natal growth retardation, characteristic facies, microcephaly, mental retardation and poor feeding. Because of the eczema which was present in half of the cases after 4 years of age, it cannot be mistaken for the more frequent fetal alcohol syndrome. We report 5 cases, among whom two sibs, confirming the recessive autosomal mode of inheritance and the necessity for genetic counseling.

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Year:  1991        PMID: 1793348

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


  3 in total

1.  Anesthesia of a patient with Dubowitz syndrome -A case report-.

Authors:  Min Kee Lee; Yong Seock Lee
Journal:  Korean J Anesthesiol       Date:  2010-05-31

2.  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

3.  Dental and craniofacial characteristics in a patient with Dubowitz syndrome: a case report.

Authors:  Andrea Ballini; Stefania Cantore; Domenica Tullo; Apollonia Desiate
Journal:  J Med Case Rep       Date:  2011-01-27
  3 in total

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