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A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Hair loss treatment caused more hair loss in a man.

Scientists found a gene in mice that causes early hearing loss.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Trichoscopy is crucial for diagnosing and assessing alopecia areata in children.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Higher antigliadin antibodies are linked to more severe alopecia areata, suggesting screening for celiac disease in these patients.

TTD symptoms vary widely, requiring thorough evaluations.