Congenital Atrichia: A Case Report

    Nilesh Dhanaji Kanase, Abhijit Shinde, Suresh Waydande
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    Studysummary In this report, a preterm neonate was found to have total irreversible hair loss due to congenital atrichia, confirmed by a mutation in the human hairless gene on chromosome 8p22, illustrating this rare autosomal recessive disorder.
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