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Parental socioeconomic status doesn't improve dietary habits or reduce disease severity in children with sickle cell disease.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

The condition might be caused by genetic changes after birth.

Alopecia areata is linked to blood cancers, especially in older patients, but not to most solid cancers.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

The study found that alopecia areata and hypothyroidism increase the risk of each other, but androgenetic alopecia and hypothyroidism do not.

Most hair follicle stem cells do not protect their DNA by dividing it unevenly.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Mutations in the KRT85 gene cause hair and nail problems.

A 13-year-old boy had both lichen planus and vitiligo, suggesting a possible link between the two conditions.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Non-white organ transplant patients have worse skin cancer outcomes due to later diagnosis and treatment.

The study identified key immune cell differences between mild and severe alopecia areata.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

A woman's sudden hair loss three years after a bone marrow transplant was a sign of chronic graft-versus-host disease but improved with treatment.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

SLE patients experience hair loss similar to telogen effluvium, with hair damage and immune activity at hair follicles.

A 16-year-old girl with lupus symptoms improved with treatment despite negative ANA tests.

Children with alopecia areata and their caregivers experience significant emotional and quality of life challenges.

A girl inherited excessive body hair from her mother and grandmother.