Literature DB >> 18990984

Dubowitz syndrome: a cholesterol metabolism disorder?

E Yeşilkaya1, K Karaer, A Bideci, O Camurdan, E F Perçin, P Cinaz.   

Abstract

Dubowitz syndrome (DS) (MIM#223370) (4) is a very rare genetic and developmental disorder involving multiple congenital anomalies including: 1) growth failure/short stature; 2) unusual but characteristic facial features; small triangular face, high sloping forehead, ptosis, short palpebral fissures, broad and flat nasal bridge; 3) microcephaly; 4) mild mental retardation; and 5) in at least 50% of the cases, eczema. Multiple organ systems are affected and the disorder is unpredictable and extremely variable in its expression. Here we describe a male Turkish patient who has typical and less common findings of DS with additionally persistently low serum lipid levels and an arachnoid cyst. The present patient is the second case of DS with persistently low cholesterol levels.

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Year:  2008        PMID: 18990984

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  2 in total

1.  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

2.  Dubowitz syndrome: common findings and peculiar urine odor.

Authors:  Cynthia Chehade; Johnny Awwad; Nadine Yazbeck; Marianne Majdalani; Rima Wakim; Hala Tfayli; Chantal Farra
Journal:  Appl Clin Genet       Date:  2013-10-08
  2 in total

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