Management of New Born with Harlequin Ichthyosis: A Rare Disease Condition

Wanjari, Mayur B. and Mendhe, Deeplata and Wankhede, Pratibha (2021) Management of New Born with Harlequin Ichthyosis: A Rare Disease Condition. Journal of Pharmaceutical Research International, 33 (57B). pp. 114-117. ISSN 2456-9119

[thumbnail of 4789-Article Text-6889-1-10-20221006.pdf] Text
4789-Article Text-6889-1-10-20221006.pdf - Published Version

Download (411kB)

Abstract

Harlequin ichthyosis is the most severe form of non-bullous ichthyosis, which is unusual in newborns and is usually marked by deadly excessive keratinization of the skin. Ichthyosis is a family of genetic skin disorders, characterized by dry, thickened, scaly skin with severe morbidity and mortality. The term “harlequin” derives from the facial appearance and the triangular and diamond-shaped pattern of the scaly skin. It occurs in about 1 in 300,000 births and has no known sex predilection. The disorder affects the skin in utero causing thick, horny, armory-like plates that cover the skin with contraction abnormalities of the eyes, ears, mouth and appendages. There is no specific guideline to manage the newborn of harlequin ichthyosis, in that nursing care is most important in the initial phase. There are required multi-disciplinary teams to take care of harlequin ichthyosis.

Item Type: Article
Subjects: Library Keep > Medical Science
Depositing User: Unnamed user with email support@librarykeep.com
Date Deposited: 30 Jan 2023 11:06
Last Modified: 08 Feb 2024 04:26
URI: http://archive.jibiology.com/id/eprint/71

Actions (login required)

View Item
View Item