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A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A new compound effectively inhibits human 5α-reductase 1.

New pyrazole-based inhibitors show promise for treating metabolic diseases and other conditions.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

Isotretinoin can raise CPK levels, so patients need monitoring, especially before surgery.

Blocking the enzyme that turns testosterone into DHT can safely and effectively treat enlarged prostate.

A peptide in shampoo can promote hair growth and improve hair condition.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

P311 helps skin stem cells become myofibroblast-like cells, aiding wound healing.

α-Phellandrene may help prevent hair loss by increasing growth factors and cell growth in hair cells through a specific signaling pathway.

Some medications for inflammation can cause a condition with scalp rashes and hair loss, often linked to Crohn's disease, and may require treatment changes to prevent permanent hair loss.

TRPM5 is crucial for maintaining hair growth.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Copper boosts cell growth in rabbit hair follicles.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

A young woman had a rare scalp tumor usually found in older women.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Activating PKM2 and Wnt/β-catenin signaling together can potentially enhance hair growth and could be a treatment for hair loss.

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

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

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ChatGPT 4.0 and Gemini 1.5 Flash are effective for educating patients about androgenetic alopecia, while Deepseek R1 is less reliable.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

TRPS1 loss in balding scalp areas contributes to hair loss in androgenic alopecia.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.