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The convention discussed various skin conditions and treatments, and highlighted the importance of vaccinations for patients on immune-altering medications.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

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

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

A woman with Fox-Fordyce disease had symptom relief using tretinoin cream.

The study found that long-term sun exposure does not significantly affect follicular plugs on the scalp, and the scalp's appearance is unique compared to other body parts.

Tiny infundibular cysts are the main lesions in chloracne, not comedones.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Graham-Little syndrome causes scarring hair loss and skin bumps.

Yellow dots in hair and scalp examinations are important for diagnosing different scalp conditions.

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

Vitamin D3 ointment improved skin bumps on the chin but didn't give lasting results after stopping use.

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.

Four new cases confirmed the unique features of follicular porokeratosis.

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.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

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 man with skin and hair symptoms improved partially with specific treatment.

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

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.