Search

everythinglearnresearchcommunity

for

Search:↓

Both HLA-B and MICA are independently linked to alopecia areata.

A genetic marker linked to a type of hair loss was found in most patients studied.

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

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

Early detection and stopping the drug are key to managing DRESS, and careful monitoring is important due to possible severe reactions.

The chapter explains the causes of excessive hair growth and masculinization in women and how to measure hormone levels related to these conditions.

EGCG may help treat alopecia areata by blocking certain immune responses and reducing specific harmful immune cells.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

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

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

Understanding the immune-related causes of Alopecia Areata has led to potential treatments like JAK inhibitors.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

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

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

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

Frontal fibrosing alopecia in Brazil mostly affects postmenopausal women, often linked with hypothyroidism and eyebrow hair loss.

Tofacitinib temporarily regrew hair in a man with alopecia, but its effects didn't last.

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

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

Alopecia areata causes hair loss, has no cure, and various treatments exist.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

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.

Psoriasis is linked to other autoimmune diseases and involves a specific inflammatory process.

A protein called EGFR protects hair follicle stem cells, and when it's disrupted, hair follicles can be damaged, but blocking certain pathways can restore hair growth.