Profound biotinidase deficiency in a child with predominantly spinal cord disease

Neuroscience

• Biotinidase 100%
• Spinal Cord Disease 75%
• Paraparesis 50%
• Differential Diagnosis 25%
• Missense Mutation 25%
• Hypotonia 25%
• Biotin 25%
• Seizure 25%
• Gene 25%

INIS

• diseases 50%
• mutations 50%
• spinal cord 50%
• resolution 25%
• children 25%
• biotin 25%
• dna 25%
• genes 25%
• symptoms 25%
• limbs 25%
• damage 25%

Biochemistry, Genetics and Molecular Biology

• Biotinidase 100%
• Nested Gene 25%
• Missense Mutation 25%
• Biotin 25%
• DNA Mutation 25%
• Childhood 25%