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A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A compound from Sansevieria trifasciata shows strong antibacterial effects against E. coli and S. aureus.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A man with alopecia universalis regrew hair temporarily after a bone treatment.

A special medium from stem cells significantly boosts hair growth and could help treat hair loss.

A new platinum complex was made and studied, which might help fight cancer better.

A woman's hair loss after COVID-19 was likely due to a mix of pressure-induced alopecia and acute telogen effluvium.

A man thought to have appendicitis actually had a rare pancreas-related condition.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

A mix of Platycladus orientalis leaf extract and alpha-terpineol helps mice grow hair by increasing growth factors and cell growth.

A new surgical technique effectively cures acne in most patients.

A new method effectively measures nicotine and cotinine in blood and urine for forensic analysis.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

A three-year-old girl survived a rare serious infection caused by BCG vaccination, which improved after treatment with a leprosy drug.

A new carrier improves skin delivery of tofacitinib for treating inflammatory skin diseases.

A stray cat with severe scabies recovered after 4 weeks of treatment.

A girl with type 1 diabetes developed a serious eye condition very early, suggesting the need for earlier eye checks and that early treatment can work well.

A 6-year-old girl with alopecia universalis regrew most of her hair after treatment with simvastatin/ezetimibe, minoxidil, and prednisolone.

A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A 17-year-old girl was diagnosed with a rare ovarian tumor, emphasizing the need for fertility preservation and psychosocial care.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.