Tuberous sclerosis complex: clinical features, diagnosis, and prevalence within Northern Ireland

Biochemistry, Genetics and Molecular Biology

• Prevalence 100%
• Tuberous Sclerosis 100%
• Mutation 75%
• Age 37%
• TSC2 37%
• Nested Gene 25%
• TSC1 25%
• Learning 12%
• Phenotype 12%
• Autosomal Dominant Inheritance 12%
• Mutation Rate 12%
• Genotype Phenotype Correlation 12%
• Chromosome 9 12%
• Chromosome 16 12%

Neuroscience

• Tuberous Sclerosis 100%
• Gene 25%
• Phenotype 25%
• Epilepsy 25%
• TSC1 25%
• Genotype 12%
• Learning Disabilities 12%
• Autosomal Dominant Disorder 12%
• Chromosome 16 12%
• Chromosome 9 12%

Immunology and Microbiology

• Autosomal Dominant Inheritance 14%