Harlequin Ichthyosis: A Fatal Disease
DOI:
https://doi.org/10.3329/jmj.v19i2.79392Keywords:
Harlequin ichthyosis, Autosomal recessive, BCA12 gene mutationAbstract
Harlequin ichthyosis (HI) is a rare and severe form of congenital ichthyosis that is inherited in an autosomal recessive manner. Affected newborns are frequently premature, and this illness may be fatal at birth. Severe hyperkeratosis, widespread fissuring, and varying degrees of cutaneous abnormalities are the disease's hallmarks. Here a case of a harlequin baby is reported who was born prematurely and to consanguineous parents. She had typical manifestations of harlequin ichthyosis. Conservative treatment was given, but the baby died on the eighth day of her life.
Jalalabad Med J 2022; 19 (2): 67-70
30
23
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2022 Jalalabad Medical Journal

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.