Dr. Mohamed Mansoor I Reviews

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.

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 19-year-old college athlete from Chennai suddenly developed cardiac symptoms during training. Genetic testing revealed Catecholaminergic Polymorphic Ventricular Tachycardia. Dr. Mansoor implemented beta-blocker therapy and activity restrictions, preventing potential sudden cardiac death and allowing safe continuation of studies.

A family of Syrian Christian descent from Kerala presented with multiple members affected by a mysterious neurological condition. Dr. Mansoor's team discovered a previously undocumented genetic mutation and developed a custom monitoring protocol while researching potential treatments through international collaborations.

A 38-year-old auto-rickshaw driver with limited resources came with his daughter showing signs of progressive muscle wasting. Dr. Mansoor diagnosed Duchenne Muscular Dystrophy and secured charitable funding for experimental exon-skipping therapy, significantly slowing disease progression.

A 52-year-old businessman from Mumbai with unexplained liver cirrhosis underwent genetic testing that revealed Hereditary Hemochromatosis. Dr. Mansoor's targeted phlebotomy treatment protocol reversed organ damage and transformed the patient's long-term health outlook.

A 25-year-old woman from a conservative family sought help for recurrent pregnancy losses. Chromosomal analysis revealed a balanced translocation, and with Dr. Mansoor's guidance through preimplantation genetic diagnosis, she successfully delivered a healthy baby after two years of treatment.

A 14-year-old girl from a tribal community in Odisha presented with unusual skin lesions and developmental delays. Dr. Mansoor diagnosed Xeroderma Pigmentosum and created a comprehensive sun-protection plan using locally available materials, dramatically improving her quality of life.

A 41-year-old chef from Chennai with a family history of early cardiac events underwent genetic screening that revealed Familial Hypercholesterolemia. Dr. Mansoor's aggressive lipid management plan using novel medications reduced cardiac risk by 80% within six months.

A 67-year-old retired army officer presented with atypical Parkinsonian symptoms. Genetic testing uncovered a rare GBA mutation, allowing Dr. Mansoor to tailor a treatment regimen that specifically addressed his unique variant, significantly improving motor function and slowing progression.