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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Transplanted whisker follicles caused long hair growth on the spinal cords of mice.

Human skin has less GDNF and its receptor with age.

A rare form of lupus can cause severe nerve damage and other symptoms, but treatment can help.

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

A woman with rheumatoid arthritis had a unique type of scarring hair loss not caused by infection, requiring early treatment to avoid permanent hair loss.

Lower growth factors linked to balding in androgenetic alopecia.

Type II spiral ganglion neurites avoid high concentrations of laminin and fibronectin.

A young woman with a rare hair loss condition improved with steroid and biotin treatment.

AMT may cause hair loss and changing dWAT activity could help treat it.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Alitretinoin helped clear up a skin condition called generalized granuloma annulare in an elderly man.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

VKHD and sarcoidosis may share a common cause.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Minimally invasive glaucoma surgery can effectively manage glaucoma in GAPO syndrome when other treatments fail.

Extracellular vesicles can worsen Alzheimer's but also offer potential for diagnosis and treatment.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

FFA and FAPD might be related or stages of the same disease.

Innate lymphoid cells type 1 may contribute to alopecia areata.

Reduced alpha smooth muscle actin may cause hair loss in androgenetic alopecia.

A specific gene mutation causes complete hair loss without other health issues.

Inhibiting connective tissue sheath contraction may improve hair growth in male pattern baldness.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Genetic factors might cause fibrosing alopecia linked to hair shaft abnormalities.

The mystacial pad's innervation in adult rats is more complex than previously thought.

A woman lost all her hair in one day, was diagnosed with a rare type of hair loss, and regrew it in 12 weeks with treatment.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.