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Hormonal imbalances during menopause may significantly contribute to Frontal Fibrosing Alopecia.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Psoriasis involves immune and genetic factors, and understanding these can improve treatments.

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

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

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.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

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

Celiac disease can cause skin problems that may get better with a gluten-free diet.

Mutations in the KRT85 gene cause hair and nail problems.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Blocking the ATX-LPA pathway may improve insulin sensitivity and mitochondrial function in obesity.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Tight junctions are key for skin protection and controlling what gets absorbed or passes through the skin.

Certain gene variations increase the risk of alopecia areata in Koreans.

Frontal Fibrosing Alopecia needs better diagnostics and treatments, with dutasteride showing promise.

Certain IL-18 gene variations may increase the risk of alopecia areata.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Bacteria in our hair can affect its health and growth, and studying these bacteria could help us understand hair diseases better.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

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.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

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