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Growth hormone therapy can improve symptoms and growth in children with Vitamin-D Dependent Rickets Type-2.

The visfatin GT genotype may increase the risk of Alopecia Areata.

The new assay can help develop products for hair re-growth.

Farudodstat may effectively treat alopecia areata without harmful side effects.

Certain genetic variants may increase the risk of developing PCOS.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

The combination of hair follicle stem cells and PRP shows promise for treating hair loss in Asian men and women.

New genes linked to male pattern baldness were found on chromosome 20p11.

The best speed for preparing platelet-rich plasma with PRPBAG® is 1800 rpm.

Clinical trials for hair loss in the USA show differences in participation among different races and ethnic groups.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

A new compound with strong antiandrogenic effects was found, potentially useful for treating conditions like acne and prostate cancer.

Somatic BHD mutations are rare in Japanese renal tumors.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

The Thai Society of Hair Restoration Surgery (TSHRS) is introduced.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

The treatment was effective and tolerable for advanced gastric cancer.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.