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Harlequin Ichthyosis: a case report and literature review.
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  • Abhigan Shrestha,
  • prince biswas,
  • sajina shrestha,
  • shumneva shrestha,
  • romana riyaz,
  • Muhammad Hassnain Nawaz,
  • Labiba hossainy
Abhigan Shrestha
M Abdur Rahim Medical Medical College Hospital

Corresponding Author:[email protected]

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prince biswas
Rajshahi University
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sajina shrestha
KIST Medical College
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shumneva shrestha
Tribhuvan University Institute of Medicine
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romana riyaz
Shadan Institute of Medical Sciences
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Muhammad Hassnain Nawaz
Dinajpur Medical College
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Labiba hossainy
Shaheed Ziaur Rahman Medical College
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Abstract

Harlequin Ichthyosis is a rare autosomal recessive disorder occurring in 1: 3,000,000 birth characterized by thick keratin skin with scaly appearance. Preterm deliveries, early marriage and consanguinity of marriage are some risk factors. Antenatal checkup of DNA for ABCA12 mutation helps in diagnosis but USG in places where not available.

Peer review status:Published

27 Sep 2022Submitted to Clinical Case Reports
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28 Sep 2022Submission Checks Completed
28 Sep 2022Assigned to Editor
03 Oct 2022Reviewer(s) Assigned
18 Oct 2022Review(s) Completed, Editorial Evaluation Pending
19 Oct 2022Editorial Decision: Revise Minor
23 Oct 20221st Revision Received
25 Oct 2022Submission Checks Completed
25 Oct 2022Assigned to Editor
25 Oct 2022Review(s) Completed, Editorial Evaluation Pending
25 Oct 2022Reviewer(s) Assigned
16 Nov 2022Editorial Decision: Accept
Dec 2022Published in Clinical Case Reports volume 10 issue 12. 10.1002/ccr3.6709