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Ruxolitinib helped a patient with alopecia areata regrow hair.

Certain genes are linked to the risk of developing Alopecia Areata.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

People with alopecia areata have a higher risk of heart disease.

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

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Balding people may have higher heart disease risk.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

SLE should be considered when investigating the cause of a stroke to prevent more strokes.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Careful diagnosis and management of MCTD are crucial due to potential severe complications.

Hair loss in African American women, caused by hair care, genetics, and environment, needs more research for better treatment.

Vasodilators may worsen abdominal aortic aneurysm.

C-reactive protein helps monocytes stick to blood vessel cells by causing oxidative stress.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Blocking CCR5 can prevent and improve hair loss in alopecia areata.

Alopecia areata may increase the risk of cardiovascular disease.

Mice with autoimmune hair loss showed signs of heart problems.

A specific gene mutation causes a severe skin disorder in a family.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Men with severe early-onset baldness may have worse heart artery function and stiffer arteries if they have high blood pressure.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

People with Behçet's disease can develop life-threatening lung artery aneurysms that may require surgery.