This book explores the basic concepts of genetics and heredity in human diseases. It discusses techniques like RT-PCR, karyotyping, DNA/RNA extraction, RFLP, DNA sequencing and electrophoresis, which will be helpful in clinical diagnostics for patients. The book also considers developmental anomalies and birth defects, as well as the potential for folate metabolism to act as a “risk factor” in genetic disorders.
With no approved drug for Autism, this book presents a novel approach validated by brain imaging and large clinical trials. It details a repurposed drug’s unprecedented potential to be the first pediatric treatment, describing specific cases of children who improved.
