A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited.
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ABSTRACT:
SUBMITTER: Dutta A
PROVIDER: S-EPMC4763701 | biostudies-other | 2016 Jan-Feb
REPOSITORIES: biostudies-other
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A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited.
Dutta Abhijit A Ghosh Sudip Kumar SK Ghosh Arghyaprasun A Roy Sutirtha S
Indian journal of dermatology 20160101 1
De Barsy syndrome (DBS), synonymously known as autosomal recessive cutis laxa type III, is an extremely rare condition clinically characterized by cutis laxa, a progeroid appearance, and ophthalmologic abnormalities. We present here an account of 5-year follow-up since the birth of an Indian boy with DBS, who had a few rare and unusual manifestations. In addition, our case probably represents the first reported case of DBS from India. ...[more]
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