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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

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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.

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HSL treatment speeds up hair growth and reduces oxidative stress in hair follicles of ob/ob mice.

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The prototype for analyzing skin aging works technically and clinically.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

New LSS gene variants help understand congenital hypotrichosis 14 better.

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CLASI is a valid tool for assessing skin activity and damage in lupus patients.

Recognizing and treating oral lichen sclerosus is important, but treatment guidelines are lacking.

Men with systemic lupus erythematosus often have more severe symptoms but can respond well to treatment.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A boy developed a rare skin condition after recovering from a severe skin reaction, and it improved with lotion treatment.

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JSLE patients often have more hormone and metabolism issues, so regular check-ups and preventing obesity can help.

Loliolide from Scenedesmus deserticola may help with anti-aging.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.