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The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Gene variation affects prostate issues and hair loss.

Genetic factors influence growth and brain development in children.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

A substance called prostaglandin D2 is found more in bald scalps and it stops hair from growing. Blocking its receptor could potentially treat hair loss.

Dutasteride may protect the brain in early Parkinson's disease.

Blocking CYP17A1 enzyme may help improve certain brain function issues related to dopamine.

Polydeoxyribonucleotide (PDRN) may help lighten skin and treat hyperpigmentation.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Finasteride and dutasteride reduce unwanted movements from Parkinson's disease treatment by normalizing certain brain signals.

A natural steroid in the body may protect against eye damage in glaucoma.

Microneedling with topical dutasteride improves hair growth in men with hair loss and is safe to use.

GDNF helps grow hair and heal skin wounds by acting on specific stem cells.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

IL-15 helps protect hair follicles from immune attacks and encourages hair growth.

PDGF signaling may play a role in hair growth cycle regulation.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Finasteride worsens heart damage but reduces cell toxicity caused by nandrolone decanoate.

Cells from concentrated growth factor can become different cell types.

The new compounds may be more effective and cheaper than current treatments for conditions like baldness.

Enhanced stem cells from the placenta can reduce fat cell formation in eye disease.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

The guideline provides healthcare professionals in South Africa with instructions for comprehensive, multidisciplinary gender-affirming care, including HIV prevention and treatment for transgender and gender diverse individuals.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

A new small peptide may help hair growth by activating a specific receptor and should be tested in humans.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.