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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A 65-year-old woman has a growing bald spot on her scalp.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

Alopecia areata affects 1 in 50 people, with non-White ethnic groups experiencing the most impact on mental health and work.

A humanized CXCL12 antibody may delay and treat alopecia areata by altering the immune response.

Periodontitis may increase the risk of developing alopecia areata.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

The man likely has secondary syphilis affecting his nervous system.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Androgenetic alopecia is a common hair loss condition caused by testosterone effects on hair follicles, leading to thinner, shorter, and less pigmented hair, diagnosed using scalp dermoscopy and treated with topical minoxidil, antiandrogen agents, and 5-alpha reductase inhibitors.

'Eclipta prostrata' plants in Taiwan are infected with 'Candidatus Phytoplasma aurantifolia'.

Most kids with alopecia areata have other health issues, often allergies or skin conditions.

Human Beta Defensin 1 levels do not predict the risk or severity of Alopecia Areata.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Vitiligo and alopecia areata may have similar causes despite their differences.

A 46-year-old man was diagnosed with frontal fibrosing alopecia, a condition usually seen in postmenopausal women.

IL-17 plays a key role in severe hair loss in chronic alopecia areata.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

The infant's hair loss resolved naturally by 20 months without treatment.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Rabies virus was found in specific skin cells of rabid dogs' muzzles, suggesting these cells could help diagnose rabies.

Hepatitis C treatment may trigger complete hair loss, especially in those with a history of patchy hair loss, but hair usually grows back within a year.

Temporal triangular alopecia is a harmless, non-progressive hair loss condition.

ALRV5XR effectively increases hair density in men with androgenetic alopecia without adverse effects.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Human placenta hydrolysate may help treat COVID-19 by reducing virus replication and boosting immune response.

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A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Male pattern hair loss affects up to 80% of men due to genetics and hormone sensitivity.