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A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

OCT can non-invasively diagnose follicular keratosis and other hair follicle disorders.

Tretinoin cream successfully treated a woman's skin condition called Fox-Fordyce disease.

The review found that basal cell carcinomas on the scalp are not more aggressive than those in other locations.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Trichoscopy helps tell different hair loss types apart using specific scalp and hair patterns.

Reflectance confocal microscopy helped tell periorificial dermatitis apart from similar skin conditions.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A baby with KID syndrome died from infections and organ failure at 18 months old.

The document concludes that different patterns of hair thickness and scalp changes can help diagnose types of non-scarring hair loss.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Monilethrix causes short, fragile hair with no specific treatment available.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Dabrafenib can cause skin growths and sometimes low-grade skin cancer.

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

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

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

A 34-year-old woman had itchy black bumps on her face due to a condition called trichostasis spinulosa.

The girl has a genetic hair condition causing thin hair since childhood.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Follicular red dots can appear where alopecia areata and vitiligo overlap.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Linear lichen planopilaris can affect the trunk, not just the face.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.