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About 8% of people with systemic lupus erythematosus have chronic scarring alopecia, with certain symptoms and positive antibodies increasing the risk, while immunosuppressants may lower it.

Some children with COVID-19 develop skin symptoms linked to a severe inflammatory condition.

A woman with CCCA has hair loss due to factors like straighteners and tight hairstyles, and treatments include steroids and avoiding certain hair products.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

Early genetic testing and new therapies like secukinumab are crucial for managing Netherton syndrome effectively.

Sebaceous glands are often preserved and PPARy expression is constant in some cases of Central Centrifugal Cicatricial Alopecia.

Treatment reduced cystic lesions but didn't change existing Nevus Comedonicus.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Hair-Thread Tourniquet Syndrome is a rare condition where hair or thread tightly wraps around a child's body part, requiring quick treatment to prevent damage.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

The study found that polymorphous light eruption varies among patients and can be distinguished from benign summer light eruption by the time it takes for symptoms to appear after sun exposure.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Satoyoshi syndrome can cause eye problems like uveitis and retinal vein issues.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

The study concludes that long COVID recovery involves time, various treatments, and a strong patient-provider relationship.

A girl had two rare hair conditions that helped understand their overlap.

The CLASI is a reliable tool for measuring the severity of cutaneous lupus erythematosus.

Itch is a common symptom in patients with chronic venous insufficiency, often worsening with standing or sitting and occurring mostly in the evening or at night.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

CO2 laser-associated PDT effectively treated therapy-resistant folliculitis decalvans.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

The new classification system for skin disorders emphasizes the importance of understanding a patient's awareness of their condition for better treatment.

Psoriasis can cause rare vulval scarring.