What is it about?
Harlequin Ichthyosis is an extremely rare genetic skin disorder that is associated with a high mortality rate. It is the most severe phenotype of congenital ichthyosis and affects both sexes equally. This paper tries to highlight if there could be an association between Harlequin Ichthyosis neonate and parental psoriasis.
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Photo by Jonathan Borba on Unsplash
Why is it important?
This paper may add to the collective knowledge of this very rare disorder.
Perspectives
Writing this article was a great pleasure as I was the first author of the first published case of Harlequin Ichthyosis in Syria (the country where the case was reported).
Jacob Al-Dabbagh
Read the Original
This page is a summary of: Harlequin ichthyosis: A case image from Syria, Clinical Case Reports, October 2022, Wiley,
DOI: 10.1002/ccr3.6389.
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