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Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Acne was the most common skin problem in kids, with other conditions like warts and eczema also frequent, varying by age and gender.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Botulinum toxin shows promise for various skin conditions but requires more research for confirmation and standardized use.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Understanding genetics is crucial for treating heart and skin diseases.

Botulinum toxin has potential for treating various skin conditions and improving wound healing.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Effective treatment for hidradenitis suppurativa varies, with antibiotics commonly used and surgery as an option, but no single method is universally successful.

Nails can reveal important health information about skin and body conditions.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Activating NRF2 might help treat hair disorders by improving antioxidant defenses.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

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

Botulinum toxin type A significantly reduces scalp psoriasis severity compared to placebo.

The document lists various dermatology topics, treatments, and diagnostic methods.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Loss of Desmocollin 3 in mice causes skin blisters and hair loss.

Recent progress has been made in understanding inherited hair and nail disorders.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.