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People with Lichen Planopilaris are more likely to have autoimmune diseases, especially Systemic Lupus Erythematosus, and less likely to have diabetes and some other common conditions.

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

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

People with cutaneous Lichen Planus are more likely to have Metabolic Syndrome and related conditions like high cholesterol, diabetes, and high blood pressure.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

A new syndrome may link skin, growth, mental, and hair issues.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Lipid–polymer hybrid nanoparticles can improve genome editing delivery and outcomes.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Lrig1 and Lgr6 stem cells help maintain hair follicles and influence skin cancer development.

Immune system failure in hair follicles causes lichen planopilaris, leading to hair loss.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.