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The review concluded that reporting on PRP therapy is often incomplete, leading to uncertainty about its effectiveness.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Next-generation sequencing greatly improves understanding and treatment of genetic hair disorders.

A girl had two rare hair conditions that helped understand their overlap.

MicroRNAs and AI can improve cashmere goat hair quality and aid in hair disorder diagnosis.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Wnt signaling is crucial for skin, hair, and nail health and regeneration.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Combined finasteride and spironolactone therapy significantly improves quality of life in women with PCOS.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

The guideline refines PCOS diagnosis, promotes a healthy lifestyle, reviews treatments, and stresses long-term follow-up.

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Disease-specific tools better assess quality of life in alopecia areata patients.

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Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

All four treatments for early rheumatoid arthritis had similar and mostly mild side effects.

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Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Both HPSAM and PLS methods accurately measure minoxidil and tretinoin concentrations.

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Low oxygen levels affect the behavior of certain proteins in human skin cells.

Patients with psoriasis ranked symptom control and treatment efficacy as most important for their care.

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Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

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