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New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Different types of dog hair loss are linked to problems starting the hair growth phase and early hair cycle ending.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

LIPH mutations cause woolly hair in some Chinese people.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

SOX10 in hair follicles is linked to inflammation in alopecia areata.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.