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

The conference highlighted new diagnostic tools, the role of genetics in hair loss, and emerging treatments.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Prolactin may play a significant role in skin and hair health and could be a target for treating skin and hair disorders.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Leptin affects skin and hair health and may worsen some skin conditions, but more research is needed to understand its full impact.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

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

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.