Dr. Srikanth KP Reviews

A 7-year-old girl from an affluent tech-expat family presented with recurrent abdominal pain and failure to thrive. Dr. Srikanth KP discovered an unusual case of eosinophilic esophagitis triggered by multiple food allergies. After implementing a strict elimination diet and targeted medication, she showed remarkable improvement within 3 months, with her weight catching up to the 50th percentile.

A 12-year-old boy from a rural farming family arrived with severe jaundice and fatigue. Diagnostic workup revealed Wilson's disease, previously undiagnosed despite family history. Dr. Srikanth initiated chelation therapy and coordinated with a nutritionist to create an affordable low-copper diet. The patient's liver functions normalized after 6 months of dedicated treatment.

A 3-year-old from an urban middle-class family presented with chronic diarrhea and developmental delays. Dr. Srikanth diagnosed a rare case of congenital sucrase-isomaltase deficiency through specialized testing. With enzyme replacement therapy and dietary modifications, the child's symptoms resolved completely within 4 weeks, allowing normal developmental progression.

A 15-year-old athlete from an upper-middle-class family developed sudden liver inflammation during sports training. Dr. Srikanth identified autoimmune hepatitis triggered by intense physical stress. Treatment involved corticosteroids and immunosuppressants, with the patient returning to modified athletic activities after 8 months of careful management.

An 8-month-old infant from a migrant worker family presented with severe malnutrition and persistent vomiting. Diagnosis revealed pyloric stenosis complicated by electrolyte imbalance. Dr. Srikanth performed a successful pyloromyotomy and coordinated social services for nutritional support. Full recovery was achieved within 2 weeks post-surgery.

A 10-year-old girl from a single-parent household presented with cyclical vomiting syndrome that had been misdiagnosed as migraines. Dr. Srikanth implemented a comprehensive management plan including antiemetics, lifestyle modifications, and psychological support. The vomiting episodes reduced from weekly to quarterly within 3 months.

A 5-year-old boy from an affluent family developed acute liver failure after accidental medication ingestion. Dr. Srikanth led the intensive care team through complex management including N-acetylcysteine protocol and monitored the child's remarkable spontaneous regeneration without requiring transplantation.

A 14-year-old from a low-income family presented with chronic abdominal pain and was found to have Helicobacter pylori infection resistant to first-line treatment. Dr. Srikanth designed a tailored antibiotic regimen based on sensitivity testing and provided medication through hospital assistance programs, achieving eradication in 3 weeks.

A 2-year-old adopted child from overseas presented with severe growth failure and steatorrhea. Dr. Srikanth diagnosed giardiasis with secondary lactose intolerance. Treatment involved antiparasitic medication and temporary lactose-free formula, with catch-up growth observed within 6 weeks of treatment.

A 6-year-old from a professional family presented with recurrent pancreatitis. Genetic testing revealed a novel mutation in the PRSS1 gene. Dr. Srikanth implemented preventive measures including dietary modifications and enzyme supplements, preventing further attacks for over 12 months of follow-up.

A 9-year-old boy from a tribal community presented with hepatomegaly and was diagnosed with visceral leishmaniasis. Dr. Srikanth coordinated with infectious disease specialists to administer liposomal amphotericin B, achieving complete parasite clearance and liver size normalization within 2 months.

A 13-year-old girl with cerebral palsy from a middle-class family developed severe GERD affecting her nutrition. Dr. Srikanth performed endoscopic fundoplication and created a specialized feeding protocol, resulting in improved weight gain and reduced aspiration episodes within 4 weeks.

An 11-month-old from a suburban family presented with intractable diarrhea. Dr. Srikanth diagnosed congenital chloride diarrhea through sweat testing and genetic confirmation. Treatment with electrolyte replacement and indomethacin resulted in normal bowel movements within 10 days.