Dyschromatosis Universalis Hereditaria: Report of a Case and Review of the Literature

    November 2002 in “ Pediatric Dermatology ”
    Khalid Al Hawsawi, Khalid Al Aboud, V. Ramesh, Daifullah Al Aboud
    TLDR A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.
    The document described a case of dyschromatosis universalis hereditaria in a 19-month-old Saudi Arabian girl who exhibited no associated defects, and none of her family members were affected. The report also reviewed similar cases from countries outside the Far East, where the disease was initially described.
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