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Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

Combined BRAF and MEK treatment increases rash risk but reduces other skin issues compared to BRAF alone.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Rubbing or pressing on the face can cause small bumps, and changing posture along with certain creams can improve them.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

The document concludes that fexofenadine reduces inflammation in chronic hives, cholestyramine helps half of pregnant women with itchy rashes, and relaxing incisions are a good alternative in facial surgery for the elderly.

Brodalumab effectively treated a man's severe hand and foot psoriasis.

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.

Some treatments can improve skin's defense against damage, but overuse may cause other skin problems.

Nrf2 helps protect skin from damage but too much can cause skin problems.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

Best treatment for Frontal Fibrosing Alopecia is 5-alpha-reductase inhibitors and intralesional corticosteroids.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

43.1% of rabbits in Mosul City had mange, with Sarcoptes scabiei var. cuniculi being the most common.

The study concluded that Acral lick dermatitis is most common in young male Labrador retrievers, often caused by psychological factors, and leads to skin inflammation and stress-related blood changes.

The dog's hair loss healed on its own without treatment.

Eating high glycemic foods and drinking milk may worsen acne by increasing insulin and IGF-1 levels.

Horizontal sections of scalp biopsies are good for diagnosing Central Centrifugal Cicatricial Alopecia and help customize treatment.

Anti-cancer treatments can cause reversible hair loss, skin sensitivity, pigmentation changes, nail damage, and skin reactions, with a need for more research on managing these side effects.

Obesity is linked to skin conditions like acanthosis nigricans and skin tags, which may indicate high insulin levels.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The study found that Temporal Triangular Alopecia often starts in early childhood, mainly affects the left side of the scalp, and has no effective treatment except surgery.

The study found that Temporal Triangular Alopecia often starts in early childhood, while Folliculitis Decalvans is characterized by tufted hairs and redness around hair follicles.

People with Down's syndrome are more likely to have syringomas.

Certain medications can reduce mortality risk in COPD patients, but others can increase risks of cardiovascular issues, postoperative delirium, and other adverse effects.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.