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      1 citations , October 2000 in “Journal of Investigative Dermatology”
      The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

      research Congenital atrichia with papular lesions

      4 citations , January 2020 in “Dermatology Online Journal”
      In this report, a 1-year-old boy with congenital atrichia with papular lesions was found to have a complete absence of scalp and body hair and keratin-filled cysts due to a mutation in the hairless gene.

      research FOXN1 deficient nude severe combined immunodeficiency

      32 citations , January 2017 in “Orphanet journal of rare diseases”
      This article reviews the genetic basis, diagnostic approaches, and treatment options for nude severe combined immunodeficiency, but does not present any new research findings.

      research Congenital atrichia with papular lesions

      8 citations , January 2014 in “Indian Journal of Paediatric Dermatology”
      This case report describes a 4-year-old boy with congenital alopecia characterized by complete irreversible hair loss and papular lesions associated with keratin-filled cysts.
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      If You Have DUPA, PLEASE READ THIS: Everyone Should Be Scalp Biopsied

      community If You Have DUPA, PLEASE READ THIS: Everyone Should Be Scalp Biopsied

      in Research  830 upvotes 2 years ago
      Scalp biopsies are crucial for diagnosing hair loss conditions like Diffuse Unpatterned Alopecia (DUPA) and retrograde hair loss, as treatments like finasteride and dutasteride may not be effective if other conditions are present. Combining PPAR-GAMMA agonists with retinoids could improve treatments for conditions like Lichen Planopilaris.
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