Clinical Case Reports (Oct 2022)

Harlequin ichthyosis: A case image from Syria

  • Jacob Al‐Dabbagh,
  • Rajaa Daabool,
  • Reem Hatem,
  • Lina Al‐Soufi

DOI
https://doi.org/10.1002/ccr3.6389
Journal volume & issue
Vol. 10, no. 10
pp. n/a – n/a

Abstract

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Abstract Harlequin ichthyosis is a rare autosomal recessive congenital ichthyosis with a distinct phenotypic appearance. It associated with a high mortality rate and affects both sexes equally. We report a harlequin fetus with a history of scalp psoriasis in his mother. The neonate was born to consanguineous parents who had a previous female baby that was diagnosed with harlequin ichthyosis.

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