Academic Journal

Harlequin Ichthyosis – Genetic and Dermatological Challenges: A Case Report and Literature Review

التفاصيل البيبلوغرافية
العنوان: Harlequin Ichthyosis – Genetic and Dermatological Challenges: A Case Report and Literature Review
المؤلفون: Brikene Elshani, Astrit M. Gashi, Besa Selimi, Arion Elshani
المصدر: International Journal of Biomedicine, Vol 14, Iss 1, Pp 182-186 (2024)
بيانات النشر: International Medical Research and Development Corporation, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
مصطلحات موضوعية: harlequin ichthyosis, ectropionm, scaly skin, consanguinity, abca12 gene, Medicine
الوصف: Harlequin ichthyosis (HI) is an extremely rare and severe genetic skin disorder characterized by thick, diamond-shaped scales covering the body, often giving the appearance of a harlequin costume. This paper provides an overview of the genetic and dermatological aspects of HI, delving into its etiology, clinical manifestations, and management. The genetic underpinnings of HI involve mutations in the ABCA12 gene, leading to impaired skin barrier function and abnormal keratinization. Understanding the molecular basis of the disorder is crucial for accurate diagnosis and potential therapeutic interventions. Clinically, HI presents challenges related to skin integrity, thermoregulation, and potential complications, such as infections. The management of HI requires a multidisciplinary approach involving dermatologists, geneticists, and other healthcare professionals. Supportive care, including emollients, careful bathing, and prevention of infections, is essential to improve the quality of life for individuals affected by this condition. Despite its rarity and severity, advancements in medical research and genetic therapies offer hope for improved treatments and interventions. This paper aims to contribute to the collective understanding of HI, fostering ongoing research and compassionate care for those living with this unique and challenging dermatological condition. We presented a premature eutrophic harlequin baby, born at 32+ weeks of gestation via emergency C-section. A clinical diagnosis was established minutes after birth, based on the typical features of HI, from scaly skin, marked fissures, and limbs in flexion contractures to prominent eclabium and bilateral ectropion.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2158-0510
2158-0529
Relation: http://www.ijbm.org/articles/i53/ijbm_14(1)_cr7.pdf; https://doaj.org/toc/2158-0510; https://doaj.org/toc/2158-0529
DOI: 10.21103/Article14(1)_CR7
URL الوصول: https://doaj.org/article/2b662e6f51064a3b9b9eb223606a47ba
رقم الانضمام: edsdoj.2b662e6f51064a3b9b9eb223606a47ba
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21580510
21580529
DOI:10.21103/Article14(1)_CR7