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  2. Werewolf syndrome: Babies in Spain develop rare disease after ...

    www.aol.com/news/werewolf-syndrome-babies-spain...

    More than a dozen babies in Spain have been diagnosed with a rare "werewolf syndrome" after taking contaminated medicine. ... Lalit Patidar, a 13-year-old boy with a genetic form of hypertrichosis.

  3. Hypertrichosis - Wikipedia

    en.wikipedia.org/wiki/Hypertrichosis

    Hypertrichosis is an abnormal amount of hair growth over the body. [1] [2] ... at least 17 Spanish children have developed so-called “werewolf syndrome”, Spain's ...

  4. Prepubertal hypertrichosis - Wikipedia

    en.wikipedia.org/wiki/Prepubertal_hypertrichosis

    Prepubertal hypertrichosis, also known as childhood hypertrichosis, is a cutaneous condition characterized by increased hair growth, found in otherwise healthy infants and children. [ 1 ] [ 2 ] Prepubertal hypertrichosis is a cosmetic condition and does not affect any other health aspect.

  5. Bearded lady - Wikipedia

    en.wikipedia.org/wiki/Bearded_lady

    A bearded lady (or bearded woman) is a woman with a naturally occurring beard normally due to the condition known as hirsutism or hypertrichosis. Hypertrichosis causes people of either sex to develop excess hair over their entire body (including the face), while hirsutism is restricted to females and only causes excessive hair growth in the ...

  6. 13-year-old boy has rare condition that causes thick hair to ...

    www.aol.com/news/13-old-boy-rare-condition...

    13-year-old Lalit Patidar from central India was given the nickname ''wolf boy'' after the effects of a rare condition, known as hypertrichosis, caused him to grow hair all over his face ...

  7. Hair disease - Wikipedia

    en.wikipedia.org/wiki/Hair_disease

    Hypertrichosis is any place of the body where there is more hair growth than is typically seen in people of the same age, race, and sex, excluding androgen-induced hair growth. [ 4 ] Hypotrichosis

  8. Cantú syndrome - Wikipedia

    en.wikipedia.org/wiki/Cantú_syndrome

    Cantú syndrome is a rare condition characterized by hypertrichosis, osteochondrodysplasia, and cardiomegaly. [ 6 ] [ 5 ] Fewer than 50 cases have been described in the literature; they are associated with a mutation in the ABCC9 -gene that codes for the ABCC9-protein.

  9. Barber–Say syndrome - Wikipedia

    en.wikipedia.org/wiki/Barber–Say_syndrome

    Barber-Say syndrome (BSS) is a very rare congenital disorder associated with excessive hair growth (hypertrichosis), fragile skin, eyelid deformities , and an overly broad mouth (macrostomia). [ 1 ] Barber-Say syndrome is phenotypically similar to Ablepharon macrostomia syndrome , which is also associated with dominant mutations in TWIST2 .