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Both Th1 and Th2 immune responses are increased in alopecia areata, with Th2 response more strongly linked to how severe the disease is.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

Vitamin B12 deficiency can cause reversible skin darkening.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.

Natural feedstuffs help reduce muscular dystrophy in rabbits more than selenium or vitamin E alone.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

Vitamin C deficiency can persist in high-risk patients despite supplementation.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Ritlecitinib may cause serious side effects like blood clots in alopecia areata patients.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

Low serum ferritin levels are linked to more severe and longer-lasting alopecia areata in children.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Patients with alopecia areata may have lower vitamin D levels than healthy people.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Alopecia areata patients often have low vitamin D levels.

Alopecia areata may involve stress-related changes affecting hormone receptors, leading to reduced cortisol production.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.