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The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

The exact cause of frontal fibrosing alopecia is unknown, but it's not likely due to sunscreen.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

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

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

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

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

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

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

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

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

New treatments targeting T-cell pathways are needed for better alopecia areata management.

Patients with acne vulgaris have lower serum irisin levels.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Hypothyroidism may cause certain types of hair loss.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

Our microbiome may affect the development of the hair loss condition Alopecia Areata, but more research is needed to understand this relationship.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

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

People with autoimmune skin diseases often have hearing problems and should get their hearing checked early.

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

People with autism are more likely to develop alopecia areata than those without autism.

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

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

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

HLA-DRB5 and other genes may be linked to alopecia universalis.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.