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Erosive palmoplantar lichen planus in North-East India mainly affects the feet and often involves nails, with unique inflammatory skin changes.

Diagonal earlobe crease and lipoprotein(a) together help diagnose coronary heart disease.

Laminin 332 is essential for normal skin cell behavior and structure.

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

Pressure from surgical headrests can cause temporary hair loss in liver donors.

Lichen Planopilaris in teens is rare, often misdiagnosed, and responds well to steroids.

Lichen planus is linked to several autoimmune diseases.

PDLLA filler can improve hair thickness and shine by reducing age-related hair decline.

Accurate early diagnosis of Lichen Planopilaris is crucial to prevent permanent hair loss.

A specific drug can help treat Lichen Planopilaris, a condition causing permanent hair loss.

Avoiding certain allergens in personal care products may improve symptoms for some patients with lichen planopilaris or frontal fibrosing alopecia.

Up to 10% of hair loss patients might have early signs of a condition called Lichen Planopilaris.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Women with lichen planopilaris often have thyroid disease, depression, anxiety, and may respond to treatment with slowed disease progression.

Eyelash drooping is linked to eyelid function and the presence of a double eyelid in Asians, and should be considered in eyelid surgery.

Adipose tissue-derived exosomes may help treat lichen planopilaris and preserve hair.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A child had a rare case of scarring hair loss with skin disease, which is hard to treat and stressful.

Repeated biopsies are crucial for managing lupus panniculitis when initial treatments fail.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.

Lipin-1 is important for skin cell differentiation and skin barrier function.

CCCA and LPP may be related hair loss conditions influenced by genetics and environment, needing early treatment.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Lhx2 helps retinal cells respond to signals for eye development.