Dubowitz Syndrome

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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Other congenital malformations

OMIM Number

223370

Mode of Inheritance

Autosomal recessive

Description

Dubowitz syndrome is a rare developmental disorder characterised by intrauterine growth retardation, microcephaly, intellectual disability, eczema and distinct facial dysmorphia. 

Epidemiology in the Arab World

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Other Reports

Lebanon

Chehade et al, 2013, described a 5-year-old Lebanese girl with Dubowitz syndrome. Apart from the typical features of facial dysmorphism, eczema, microcephaly, and developmental and growth delay, the patient also had an uneplained odorous urine. 

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