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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

A rare EGFR mutation in newborns leads to severe health issues and early death.

The study provides exploratory findings on miRNA changes in female hair loss.

Blocking IL-1 could help treat some hair loss conditions; alopecia affects liver detox systems; spironolactone is better than finasteride for female hair growth; focusing on the catagen hair phase could lead to new alopecia treatments.

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A specific gene mutation causes a rare hair loss condition in a Chinese patient.

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Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

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Cantú syndrome is caused by mutations in the ABCC9 gene.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Finasteride helps female-pattern hair loss.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.