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The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.