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Some leukemia treatments can cause skin reactions similar to keratosis pilaris.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

The laser treatment effectively and safely improved keratosis pilaris.

Four new cases confirmed the unique features of follicular porokeratosis.

Benign tumors from hair follicles can look like other skin cancers but have distinct features under dermoscopy.

EFFC might be common but underreported.

The four patients have a unique type of ichthyosis affecting hair follicles.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Acitretin effectively improved the woman's skin condition.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

The new treatment improved keratosis pilaris symptoms and mood in 28 days.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

Homeopathic treatment with Arsenicum album improved keratosis pilaris symptoms in one case.

Trichoscopy is a useful method for identifying primary cicatricial alopecias and their specific types.

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

Reducing gefitinib dosage improved hair loss, but scarring remained.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Dermoscopy helped diagnose discoid lupus erythematosus in two patients without needing skin biopsies.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Trichoscopy helps diagnose and understand Discoid Lupus Erythematosus on the scalp by identifying specific patterns.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Melatonin helped some Pomeranian dogs regrow hair, but it wasn't linked to estrogen receptors.

Acne is caused by increased sebum, abnormal skin shedding, bacteria, and inflammation, not dirt; treatments vary from creams to antibiotics or isotretinoin, with severe cases needing a dermatologist's care.