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FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

There's a red birthmark on the scalp.

PRP injections for hair loss may cause scalp nodules that can persist but often regress on their own.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Baricitinib was effective in treating both early and late onset alopecia areata.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Carbon black nanoparticles can harm liver and kidney function in mice.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

The study created special nanoparticles that effectively deliver an anti-inflammatory drug to treat skin inflammation in psoriasis.

Baricitinib treatment can help regrow scalp hair and eyebrows or eyelashes in people with severe alopecia areata.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Kerion is a rare but serious scalp infection that needs proper treatment.

Trapa bispinosa Roxb. extract may help reduce prostate size and cell growth in BPH.

Genetic analysis is crucial for diagnosing ectodermal dysplasia syndromes, and new therapies may help improve skin issues.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

Chemotherapy caused the patient's hair to have alternating thick and thin segments.

Brain-Derived Neurotrophic Factor (BDNF) slows down hair growth and promotes hair follicle regression.

The updated NPRT system now covers different types of hair loss in men and women.

BIVV009 is a safe treatment for bullous pemphigoid that reduces C3 deposition without harmful side effects.

A young man was unexpectedly diagnosed with basal cell carcinoma after a scalp examination and confocal microscopy.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Biotinidase deficiency can be easily diagnosed and treated with biotin to prevent serious harm.

Combining fat grafts with botulinum toxin helps improve Raynaud's symptoms.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A specific gene mutation causes severe skin and nail issues and hair loss.