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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Alopecia areata patients show increased inflammation and OX40 activation, suggesting a new treatment target.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Early detection and infection prevention are crucial for improving survival in pediatric lupus patients with aplastic anemia.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

A postmenopausal woman's excess male hormone symptoms were caused by a rare adrenal gland tissue in her ovary.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.