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Harlequin Ichthyosis: A Case Report
Shoaib Akhtar1, Adeel Anwaar2, Inam Ul Haq3
1Rahbar Medical and Dental College Lahore Pakistan.
None:
Harlequin ichthyosis (HI) is a genetic disorder caused by ABCA12 gene mutations, presenting with thick, scaly skin and deep fissures. Early recognition, intensive neonatal care, and multidisciplinary management are crucial for improving survival and quality of life. Treatment focuses on skin hydration, infection prevention, and supportive care to manage symptoms effectively.
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