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Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

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INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

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Certain gene variations are found in people with polycystic ovary syndrome.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

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PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

The scraggly mutation causes hair loss and skin defects in mice.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

ESR2 gene linked to female-pattern hair loss.

New genetic mutations linked to rare skin disorders were found in three newborns.

An extract from Quercus acutissima bark was found to reduce sebum production and block an enzyme linked to acne.

Certain genetic variations are linked to hair loss in Mexican men.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

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Seborrheic dermatitis was most common in late adults and toddlers from 2016 to 2019.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

ALRN-6924 may prevent hair loss caused by chemotherapy.