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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Antibiotics often cause skin reactions, making them a major health concern.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Transplant success has improved with better immunosuppressive drugs and donor matching.

COVID-19 vaccination does not significantly increase the risk of developing alopecia areata.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

JAK inhibitors show promise in effectively treating hair loss from alopecia areata.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

CD3+ T-cell presence is a reliable marker to tell apart alopecia areata from pattern hair loss.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Recent selection on immune response genes was identified across seven ethnicities.

Hypothyroidism may cause certain types of hair loss.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

The formula YH0618 can reduce the harmful side effects of the chemotherapy drug Doxorubicin and protect healthy cells.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Pregnancy can cause skin changes and conditions that need correct diagnosis and treatment for the health of the mother and baby.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

The conclusion is that understanding the complex relationship between allergies, autoimmunity, and psychological factors is key to treating skin disorders with itching.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

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 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.