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Harlequin Ichthyosis: A case image from Syria
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  • Jacob Al-Dabbagh,
  • Rajaa Daabool,
  • Reem Hatem,
  • Lina Al-Soufi
Jacob Al-Dabbagh
Directorate of Health of Latakia, National Hospital of Latakia

Corresponding Author:[email protected]

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Rajaa Daabool
Directorate of Health of Latakia, National Hospital of Latakia
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Reem Hatem
Directorate of Health of Latakia, National Hospital of Latakia
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Lina Al-Soufi
Directorate of Health of Latakia, National Hospital of Latakia
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Abstract

Harlequin ichthyosis is a rare autosomal recessive congenital ichthyosis with a distinct phenotypic appearance. We report a male baby with harlequin ichthyosis who was born to consanguineous parents that have a previous female baby who was diagnosed with harlequin ichthyosis.

Peer review status:Published

09 Jul 2022Submitted to Clinical Case Reports
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13 Jul 2022Submission Checks Completed
13 Jul 2022Assigned to Editor
21 Jul 2022Reviewer(s) Assigned
24 Jul 2022Review(s) Completed, Editorial Evaluation Pending
02 Sep 2022Editorial Decision: Revise Minor
07 Sep 20221st Revision Received
09 Sep 2022Submission Checks Completed
09 Sep 2022Assigned to Editor
09 Sep 2022Review(s) Completed, Editorial Evaluation Pending
16 Sep 2022Editorial Decision: Accept
Oct 2022Published in Clinical Case Reports volume 10 issue 10. 10.1002/ccr3.6389