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The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Enlarged sweat gland ducts may indicate scarring hair loss.

A 16-year-old boy had pernicious anemia, autoimmune hemolytic anemia, and later developed alopecia areata.

The condition is harmless, doesn't worsen, and needs no invasive treatment.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Some people with chronic hair loss may have thyroid autoimmunity.

People with alopecia areata may have a higher risk of thyroid diseases.

A new genetic mutation was found causing hair and eye issues in a boy.

Glucocorticoids and thyroid hormones together are essential for fetal fat development.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Alopecia areata can be an early sign of Hodgkin’s lymphoma and may improve with lymphoma treatment.

Thyroid hormone treatments help thyroidectomized rats grow normally.

Allergies, especially dust mite allergy, may worsen alopecia areata, and desensitization could help reduce its severity.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

A woman's rare hair loss condition improved on its own, suggesting this type might recover like common cases.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

Alopecia areata incognito in children can be effectively treated with triamcinolone acetonide and supplements, leading to full hair regrowth.

Children with Alopecia Areata often have lower vitamin D and B12 levels and higher thyroid activity.

Skin and mucous membrane issues are common in kids after bone marrow transplants, so careful monitoring is crucial.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Canine hypothyroidism often causes skin issues like hair loss.

Targeting specific T cells may help treat alopecia areata.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Using thigh skin, doctors successfully rebuilt a woman's scalp after removing a large tumor, with no tumor return after 8 months.

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

The boy's symptoms suggest a possible new medical condition.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

β-thymosin in invertebrates is more complex and diverse than in vertebrates.