Harlequin Ichthyosis: A case image from Syria
- Jacob Al-Dabbagh
, - Rajaa Daabool,
- Reem Hatem,
- Lina Al-Soufi
Jacob Al-Dabbagh
Directorate of Health of Latakia, National Hospital of Latakia
Corresponding Author:jacobaldabbagh0@gmail.com
Author ProfileRajaa Daabool
Directorate of Health of Latakia, National Hospital of Latakia
Author ProfileReem Hatem
Directorate of Health of Latakia, National Hospital of Latakia
Author ProfileLina Al-Soufi
Directorate of Health of Latakia, National Hospital of Latakia
Author ProfileAbstract
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.09 Jul 2022Submitted to Clinical Case Reports 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
