Harlequin Ichthyosis: A Fatal Disease

Authors

  • Zainab Rahman Registrar, Department of Paediatrics , Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet
  • Archana Dev Associate Professor, Department of Paediatrics , Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Tofayel Ahmed Registrar, Department of Paediatrics, Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet
  • Rabaka Sultana Indoor Medical Officer, Department of Paediatrics , Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet
  • Joyoshree Paul Indoor Medical Officer, Department of Paediatrics , Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet
  • Nahidur Rahman Indoor Medical Officer, Department of Paediatrics , Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet

DOI:

https://doi.org/10.3329/jmj.v19i2.79392

Keywords:

Harlequin ichthyosis, Autosomal recessive, BCA12 gene mutation

Abstract

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

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Published

2025-03-04

How to Cite

Rahman, Z., Dev, A., Ahmed, T., Sultana, R., Paul, J., & Rahman, N. (2025). Harlequin Ichthyosis: A Fatal Disease. Jalalabad Medical Journal, 19(2), 67–70. https://doi.org/10.3329/jmj.v19i2.79392

Issue

Section

Case Report