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Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

A woman's hair turned white after taking a cancer drug called dasatinib.

Lupus erythematosus panniculitis on the scalp can cause unique geometric hair loss patterns.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

Loricrin affects skin immune function and homeostasis.

Early recognition and evaluation of nevus sebaceus are crucial to detect and manage potential cancerous changes.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Doctors should consider comedonic discoid lupus erythematosus to avoid misdiagnosis.

Follicular mucinosis in a 15-year-old is usually harmless but needs monitoring for possible lymphoma.

A fungus ball in the lung can cause coughing up blood in SLE patients.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Erlotinib can cause persistent excessive hair growth.

A woman's hair loss looked like a different condition due to her hairstyle, and treatment stopped further hair loss but didn't regrow hair.

Lichen planopilaris can occur with multiple autoimmune diseases.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Specific immune cells and pathways contribute to hair follicle inflammation and hair loss, suggesting potential treatments for lichen planopilaris.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

Cats infested with Lynxacarus radovskyi can lose hair without inflammation, treatable with selamectin.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

Keratoacanthomas on lips may originate differently than those on skin.

A woman got a scalp condition from using latanoprost, but it improved after stopping the drug and starting other treatments.

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

Increased LC3 gene expression may be linked to premature graying of hair.

Giant solitary trichoepithelioma is a rare, usually non-cancerous hair follicle tumor that can sometimes turn into skin cancer.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Apoptosis in hair follicles spreads through cell death signals, with stem cells slowing the process.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.