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Clinical Approach to a child with Poikiloderma: A case report
  • Samir Shrestha,
  • Sudha Agrawal
Samir Shrestha
BP Koirala Institute of Health Sciences
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Sudha Agrawal
BP Koirala Institute of Health Sciences
Author Profile

Abstract

Rothmund-Thomson Syndrome is a rare autosomal recessive condition presenting usually in infancy that can be diagnosed based on time of onset, spreading and appearance of the poikiloderma.The purpose of reporting this case is to highlight the clinical approach to a child who presents with the features of poikiloderma.

Peer review status:Published

04 Sep 2021Submitted to Clinical Case Reports
08 Sep 2021Submission Checks Completed
08 Sep 2021Assigned to Editor
16 Sep 2021Reviewer(s) Assigned
01 Oct 2021Review(s) Completed, Editorial Evaluation Pending
03 Oct 2021Editorial Decision: Revise Minor
04 Oct 20211st Revision Received
05 Oct 2021Submission Checks Completed
05 Oct 2021Assigned to Editor
05 Oct 2021Review(s) Completed, Editorial Evaluation Pending
05 Oct 2021Editorial Decision: Accept
Oct 2021Published in Clinical Case Reports volume 9 issue 10. 10.1002/ccr3.4977