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Excluding alopecia and mucous membrane components from the CLASI-A score reduces its effectiveness in capturing important disease activity.

Etanercept improved symptoms of a specific type of psoriatic arthritis in a patient who didn't respond to other treatments.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

A man developed a unique rash on his neck after taking niacinamide, and doctors recommend considering niacinamide as a cause for similar rashes and using dermatoscopy for diagnosis.

Topical tofacitinib cream may help treat certain hair loss conditions with fewer risks.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Disabling the FGF5 gene in sheep leads to longer wool.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Disposable tools could make hair restoration surgery safer and more efficient.

New mouse models of Pemphigus show severe symptoms and need better treatments.

Anti-IL-12/IL-23 antibody therapy effectively treats psoriasiform skin lesions in IBD patients.

Frontal fibrosing alopecia can be misdiagnosed as androgenetic alopecia in African American women.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

The CWARTS tool is a promising method for assessing warts and could improve treatment and research.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Patients with long COVID after Omicron had fewer hospitalizations and milder symptoms but more fatigue, insomnia, and cough compared to those with Delta.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Follicle Stimulating Hormone is important for fertility.

Genetic variations affecting skin structure play a key role in severe acne.

No treatment has been proven to effectively stop hair loss or regrow hair in Frontal Fibrosing Alopecia, and more research is needed.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.