Dr. Mohamed Mansoor I

A 45-year-old fisherwoman from coastal Tamil Nadu came with her entire family concerned about hereditary vision loss affecting multiple generations. Dr. Mansoor identified a novel mutation in the RPE65 gene and facilitated access to groundbreaking gene therapy, restoring significant vision to three family members within a year.

A 7-year-old boy from an affluent Delhi family presented with developmental delays and unusual facial features. Whole exome sequencing revealed a rare chromosomal microdeletion syndrome. Dr. Mansoor coordinated a multidisciplinary care team and implemented early intervention strategies that dramatically improved the child's cognitive function over 18 months.

A 32-year-old pregnant woman from rural Karnataka was referred after ultrasound showed fetal abnormalities. Dr. Mansoor diagnosed Thanatophoric Dysplasia through advanced genetic testing and provided compassionate counseling, helping the family make informed decisions and connecting them with support groups.

A 60-year-old retired school teacher with a complex family history of early-onset Alzheimer's sought predictive testing. Dr. Mansoor conducted comprehensive genetic counseling and testing, revealing a protective genetic variant that significantly reduced her risk, providing immense psychological relief.

A 28-year-old software engineer from Bangalore presented with unexplained muscle weakness and fatigue. After extensive genetic testing, Dr. Mohamed Mansoor diagnosed a rare mitochondrial disorder. Through personalized vitamin therapy and lifestyle modifications, the patient showed remarkable improvement within 3 months and returned to full-time work.