Keratosis Follicularis Spinulosa Decalvans: Case Report
August 2010
in “
Anais brasileiros de dermatologia/Anais Brasileiros de Dermatologia
”
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TLDR A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.
Keratosis follicularis spinulosa decalvans is a rare genetic disease characterized by follicular hyperkeratosis and cicatricial alopecia, typically starting in early childhood and worsening during adolescence. The case reported involved a child with severe cicatricial alopecia from birth, which quickly progressed to widespread scalp alopecia, resulting in limited and disappointing treatment outcomes.