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CTP-543 significantly improved eyebrow and eyelash regrowth and patient satisfaction in adults with alopecia areata.

A KRT32 gene variant causes loose anagen hair syndrome.

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CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The 800-nm pulsed diode laser is a safe and effective long-term treatment for trichostasis spinulosa in dark-skinned individuals.

Many patients with lower urinary tract symptoms also have undiagnosed erectile dysfunction, which improves with treatment.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

Telitacicept helped stabilize complement levels in a patient with lupus and thyroid cancer.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

A fast and accurate method was developed to measure alfuzosin and dutasteride in human plasma.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

A reliable, cost-effective method was developed for accurately measuring finasteride in medicines.

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A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

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Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

Incidental prostate cancer was found in 4.89% of patients undergoing surgery for benign prostatic hyperplasia.

Using a call center to collect data in a trial for eye disease in diabetics led to high response rates and very little missing information.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.