Biotinidase

A genetic disorder caused by mutations in the BTD gene. It is characterized by reduced or absent activity of the enzyme biotinidase which is responsible for the recycling of the vitamin biotin. Signs and symptoms appear in childhood and include seizures, hypotonia and developmental delays. If left untreated, it leads to vision and hearing loss, infections, alopecia and ataxia.

Disease Alternative Name

biotinidase deficiency
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Meerut
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Atrauli (Aligarh)
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Parmarth Homeopathic Ausdhalay

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Bangalore Medical College and Research Institute

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The Health City Hospital

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Maharashtra University of Health Sciences Nashik

bhms

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