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The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

A new mutation in the HR gene causes hair loss in a specific family.