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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Topical minoxidil may not improve the appearance of balding men, according to a letter in this document.

The document is a detailed medical reference on skin and genetic disorders.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Understanding skin structure and development helps diagnose and treat skin disorders.

Genetic defects and UV radiation cause skin damage and aging.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

Experts met to improve care for ichthyosis patients in Spain.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

Inflammation and Demodex mites might contribute to hair loss, and targeting them could help treat it.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

The most common skin problems in Indian children are infections and eczemas.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Certain fats in the skin help control inflammation and health, and changing these fats through diet or supplements might treat skin inflammation.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Inhibiting ALOX12 can help hair cuticle maturation by increasing S100A3 citrullination.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.