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The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

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.

Enterococcus faecalis delays wound healing by disrupting cell functions and creating an anti-inflammatory environment.

The man has a genetic skin condition called pachyonychia congenita.

Hair loss in male pattern baldness is linked to changes in specific genes and proteins that affect hair growth and scalp health.