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Keratin biomaterials from human hair help nerve regeneration by activating Schwann cells.

Tranexamic acid effectively reduced swelling episodes in a girl with a rare form of hereditary angioneurotic edema.

Azathioprine can cause hair loss and matted hair.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Lymphocytes may hinder hair stem cells, causing hair loss without scarring.

Several doctors received research grants, new workshops and conferences were announced, and new officers were elected.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

Two Hispanic women developed Plica neuropathica, a condition causing tangled hair, possibly due to hair damage and various risk factors.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

Topical glycopyrrolate lotion helped reduce excessive sweating from eating in a diabetic man.

A 16-year-old girl with lupus symptoms improved with treatment despite negative ANA tests.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

MSUD patients need careful monitoring of amino acids and zinc to prevent severe symptoms.

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

Diabetes and necrotizing fasciitis together can be deadly.

Digital gangrene can be an initial symptom of late-onset systemic lupus erythematosus.

2-DG reduces seizures by enhancing brain inhibition through specific receptor activation.

A new microneedle patch helps repair spinal cord injuries by reducing scarring and promoting nerve growth.

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

β-Catenin signaling is involved in brain cell growth after injury and could be a therapy target.

Plica neuropathica can occur with diffuse alopecia and should be considered in diagnosis.

Monilethrix causes brittle hair and hair loss, and it runs in families.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Impaired autophagy may contribute to alopecia areata.

Exosome therapy may help treat diabetic nerve damage, but more research is needed.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.