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Terminalia bellirica extracts effectively promote hair regrowth and treat androgenetic alopecia.

TSH is not reliable for detecting hypothyroidism after bariatric surgery; FT3/rT3 ratio is better.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Lower SHBG levels may increase the risk of PCOS.

Amotosalen-treated donor T-cells can prevent late CMV infection after bone marrow transplants.

Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.

Desmogleins are crucial for hair structure and growth.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

Sonic hedgehog helps hair follicle stem cells grow and can effectively regenerate hair follicles.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Supplemental testosterone may lower liver cancer risk in hepatitis C patients.

Teprotumumab for thyroid eye disease commonly causes fatigue, brittle nails, dry eyes, hair loss, muscle spasms, and dry mouth, with rare serious events like blood clots.

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

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

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The condition is linked to chromosome 12, but no mutations were found in the known genes.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

The method effectively detects MeT and TP in dried blood spots after cream application.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

Sgk3 kinase is essential for normal hair growth in mice.