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A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Scalp lesions in discoid lupus are more common in women and linked to other autoimmune diseases.

Relapsing hepatitis A can cause prolonged abnormal liver tests even without symptoms.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

The Brazilian version of the Alopecia Areata Quality of Life Index is reliable for assessing patients' quality of life.

The ethanol patch test reliably identifies ALDH phenotype.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Dupilumab may cause hair loss in some patients with severe atopic dermatitis.

A patient's skin rash did not affect the area where a previous viral rash was healing, suggesting a rare immune response.

RXRα is crucial for proper immune response and links diet to immune function.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Disease-specific tools better assess quality of life in alopecia areata patients.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Higher IL-37 levels are linked to more severe alopecia areata, but the gene variation doesn't affect disease risk.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

People with rheumatoid arthritis have a higher risk of developing alopecia areata.

Use specific tools to measure quality of life in alopecia areata patients and improve future treatments.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

DKK-1 gene linked to hair loss in AGA and AA patients; more research needed for potential therapy.