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Targeting the AhR pathway may help treat alopecia areata.

People with alopecia areata have a higher risk of stroke.

A woman lost vision in one eye after a forehead injection, but prompt treatment led to partial vision recovery.

Patients with central centrifugal cicatricial alopecia often have higher rates of metabolic, autoimmune, and atopic conditions, as well as anxiety and depression.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

Baldness is linked to a higher risk of coronary artery disease, but not to its severity.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Alopecia areata is rare in organ transplant patients and may be linked to the drug tacrolimus.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Alopecia areata involves specific T-cells, unlike androgenetic alopecia.

Different autoantibody groups in pediatric SLE are linked to specific symptoms and disease outcomes.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

A U.S. Naval fighter pilot suffered permanent vision loss in one eye due to recurrent central serous retinopathy.

The letter suggests that the study's comparison group might have affected the results and calls for larger, more detailed future research.

People with alopecia areata are more likely to get migraines, and vice versa.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

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

Zinc supplements improved the girl's skin and hair condition.

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

CDH3-related disease causes worsening eye and hair issues.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Early intervention is important for limited systemic sclerosis patients due to higher pain and ulceration risks.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The treatment successfully reopened blood flow in most patients and extended the use of their dialysis access with low risk.