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Androgen-deprivation therapies increase the risk of certain heart conditions, but testosterone treatment may help.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Iron supplements combined with Quilib lotion effectively treat hair loss in people with iron deficiency anemia.

Ptprq has multiple forms that change during inner ear development.

QR 678 and QR 678 Neo are safe and promote hair growth, potentially helping chemotherapy-induced hair loss.

The prototype for analyzing skin aging works technically and clinically.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

New laser particles can track thousands of cells in 3D models, improving single-cell analysis.

LLLT devices for hair loss need more research to define proper guidelines.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

The Thai version of the Family Dermatology Life Quality Index is a reliable and valid tool for assessing the quality of life of patients' families.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

KX-826 is safe and effectively increases hair count in men with hair loss.

New LSS gene variants help understand congenital hypotrichosis 14 better.

QR678 Neo® hair growth treatment is effective for hair loss caused by Covid-19.

The 1927 nm fractional thulium laser effectively treats acne by targeting and improving affected skin areas.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

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TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.