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A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Recent progress has been made in understanding inherited hair and nail disorders.

Modern hair restoration techniques have evolved from punch grafting to methods like micro-grafting and follicular unit transplantation, but they are labor-intensive, expensive, and can lead to patient dissatisfaction. Future treatments may involve cloned hair follicles and drugs like finasteride.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

A gene variant causes a skin and hair disorder by disrupting protein balance.

Trichoscopy can help identify systemic diseases, not just hair and scalp issues.

Some hair products can create false signs on scalp examinations, leading to wrong diagnoses.

Trichoscopy is a quick and reliable way to diagnose hair loss in women.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Female Pattern Hair Loss is linked to genetics, diet, stress, and certain health conditions.

A child with a rare vitamin D-resistant condition improved with treatment.

Trichoscopic features help diagnose and assess female pattern hair loss severity, with inflammation playing a key role.

A 13-year-old girl was diagnosed with juvenile lupus, showing only hair loss as a symptom.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Scalp melanoma is more common and easier to diagnose early in people with androgenetic alopecia due to sun damage.

Topical spironolactone works better than topical finasteride for hair loss.

Self-induced hair loss should be considered in patients with androgenetic alopecia.

The combination of PRP and triamcinolone injections improved hair growth in a man with alopecia areata.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

A rare combination of hair loss and excessive fine hair growth was found in celiac disease patients.

AA–TF#15 significantly promotes hair regrowth and could be an effective treatment for androgenic alopecia.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.