Channels Television
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Cutis Laxa: Meet The Nigerian Family Embracing Uniqueness While Living With A Rare Disorder
Posted
October 1, 2025
Views
934
October 1, 2025
934
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2:27Now PlayingIn this story, the BBC meets with a Nigerian family of seven, where three of the children were born looking strikingly different from the rest.
The family has been diagnosed with a rare genetic condition known as cutis laxa, a disorder so uncommon it affects only about one in a million people worldwide.
Despite this, they refuse to be defined by the attention, as the children continue to embrace their uniqueness with positivity.
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