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A genetic marker linked to a type of hair loss was found in most patients studied.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

New genetic mutations causing hair loss were found in a Chinese family.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.

HDMHG0401-10 improves hair loss in men with androgenetic alopecia and has no major side effects.

HS patients rarely see dermatologists, often get opiates, and need better care.

Genetic factors could lead to personalized treatments for hair loss.

HPV infection is linked to better survival in advanced anal cancer, higher radiation doses improve survival, especially in HPV-negative patients, and prostaglandin E₂ pretreatment can protect mouse hair follicles from radiation damage.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Dystonia may be part of PAS-4 and linked to immune issues.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Hirsutism in teens is often due to polycystic ovarian syndrome and needs careful assessment and support.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

No link found between hair loss severity and PSA levels in men.

Para-aminobenzoic acid in hair supplements can cause autoimmune hepatitis.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

GnRH agonists can help manage recurrent priapism in sickle cell patients, but long-term safety is unclear.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Intense exercise may increase the risk of ankylosing spondylitis in genetically predisposed adolescents.

Sacituzumab govitecan improves quality of life and symptoms in breast cancer patients, except for causing more diarrhea.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Including special area involvement helps identify more psoriasis patients who may need systemic treatment.

The nanoparticles improved hair growth and enlarged hair bulbs.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A new gene mutation linked to a skin condition was found in a Spanish family.