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Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Acne can't be cured but can be managed with treatments like benzoyl peroxide and diet changes; it's costly and can lead to scarring and mental health issues.

The conclusion is that early diagnosis of skin signs linked to diseases like Lupus, Dermatomyositis, and Rheumatoid Arthritis is crucial to prevent serious complications.

Malassezia infection may cause refractory acne, and antifungal treatments can help.

New genetic mutations linked to rare skin disorders were found in three newborns.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Reflectance confocal microscopy is useful for diagnosing and monitoring skin diseases, but it has limitations and requires expertise for correct use.

Early detection and treatment of folliculitis keloidalis can prevent disease progression.

Microneedles are promising for long-acting drug delivery and can improve patient compliance, but more data is needed to confirm their effectiveness.

Trichoscopy is a reliable method for diagnosing hair and scalp disorders quickly and non-invasively.

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.

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

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

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.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Four new cases confirmed the unique features of follicular porokeratosis.

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.

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.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.