Bart’s Syndrome Associated Corpus Callosum Agenesis and Choanal Atresia
Iranian Journal of Child Neurology,
Vol. 8 No. 4 (2014),
2 December 2014
,
Page 76-79
https://doi.org/10.22037/ijcn.v8i4.5064
Abstract
How to Cite This Article: Saeed M, Haq A, Qadir Kh.Bart’s Syndrome Associated Corpus Callosum Agenesis and Choanal Atresia. Iran J Child Neurol. 2014 Autumn;8(4): 76-79.
Abstract
Objective
Bart’s syndrome is defined as congenital localized absence of skin, and associated with epidermolysis bullosa. A newborn with Bart’s syndrome is reported because it is a very rare condition, especially when associated with corpus callosum agenesis and concomitant choanal atresia. Clinically it is characterized by raw beefy areas of denuded skin mainly on hands and feet.
We report a rare case of a term female newborn born to non-consanguineous parents who presented with congenital absence of skin in, face, trunk and extremities. To the best of our knowledge, this is the first report presenting a case of Bart’s syndrome associated with corpus callosum agenesis.
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- Bart’s syndrome
- Congenital absence of skin
- Epidermolysis bullosa
- Choanal atresia
- Corpus callosum agenesis (CCA)
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