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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

Follicular vitiligo causes hair to gray without skin color loss.

HLA-DRB5 and other genes may be linked to alopecia universalis.

The role of γδT-cells in causing alopecia areata remains unclear.

Alopecia areata can be reversed by JAK inhibitors, promoting hair regrowth.

Consider infectious diseases like visceral leishmaniasis before diagnosing autoimmune hepatitis.

People with allergies or high eosinophil levels have a higher chance of severe hair loss from alopecia areata, and sudden hair loss can indicate chronic graft-versus-host disease.

Dr. Shoji Okuda's pioneering work on hair transplantation was overlooked and could have significantly advanced the field if recognized sooner.

KFSD causes scarring hair loss and skin roughness, mainly in males.

People with autism are more likely to develop alopecia areata than those without autism.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

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

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

Women with androgenetic alopecia may have higher blood pressure levels.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Traditional oriental hair care products and Yukmijihwang-huan improved hair loss symptoms in two older men.

Tofacitinib is effective and safe for treating severe alopecia areata and related conditions.

A postmenopausal woman's masculine symptoms improved after surgery for a hormone-producing ovarian tumor.

Tacrolimus and corticosteroids can improve symptoms of Satoyoshi syndrome.

Early greying and male pattern baldness can predict heart disease in young Asian men.

8-OHdG may help diagnose and assess alopecia areata.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

No clear link between specific gene and hair loss in Mexican brothers.