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Combining platelet-rich plasma with other treatments may improve hair growth in androgenetic alopecia.

Combining platelet-rich plasma with other treatments may improve hair growth in androgenetic alopecia.

Alopecia areata involves immune system issues and specific cell types that disrupt hair growth, leading to hair loss.

Patient-reported hair improvements align with actual hair density changes, not hair width.

Free long-chain fatty acids can stimulate hair growth in mice.

Combining PRS with TAFR is promising for treating complex fistulas, with most patients achieving long-term healing.

Clove oil effectively treats cattle dermatophytosis in 7 days.

Bimatoprost helps with hair growth and eye conditions but can be costly and have side effects.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

Urologists should screen for mental health issues before and during finasteride treatment.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

PHAs are promising biodegradable materials for medical and dental uses.

Finasteride's solubility and bioavailability improved by forming solid dispersions and inclusion complexes.

Effective treatment significantly improves pododermatitis in dogs, reducing symptoms and extending remission.

COVID-19 may cause different types of hair loss, and the virus's effects on hair could help understand its impact on other body parts.

Anionic surfactants significantly improve the foaming of minoxidil gel shampoo.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A new DSG4 gene mutation causes hair defects in a young girl.

Gonadal biopsy is the best method to diagnose gonadal dysgenesis.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.