Dr. Anil Khichar Reviews

A 7-year-old boy from a remote village presented with recurrent seizures and developmental delay. Dr. Khichar diagnosed a rare metabolic disorder through advanced genetic testing. With customized dietary management and medication, the child showed remarkable improvement in cognitive functions over 6 months, enabling him to attend a special school.

An affluent family's 3-year-old daughter was brought in with persistent high fever and rash. Dr. Khichar identified Kawasaki disease and administered intravenous immunoglobulin promptly. The child recovered completely within two weeks with no coronary complications, thanks to early intervention.

A 12-year-old from an urban slum presented with severe malnutrition and recurrent infections. Dr. Khichar discovered an underlying immunodeficiency syndrome. Through nutritional rehabilitation, antibiotic prophylaxis, and family education, the patient's health stabilized over 3 months with significantly reduced hospital visits.

A newborn from a middle-class family was referred with jaundice that wasn't resolving. Dr. Khichar diagnosed biliary atresia and coordinated with surgeons for a Kasai procedure. The infant showed good bile drainage post-surgery and is under long-term follow-up for liver health.

A 5-year-old adopted child from an orphanage presented with behavioral issues and growth failure. Dr. Khichar identified reactive attachment disorder and implemented a multidisciplinary approach involving play therapy, nutritional support, and caregiver training, leading to gradual emotional and physical improvement over a year.

A teenage athlete from a wealthy background collapsed during training. Dr. Khichar diagnosed hypertrophic cardiomyopathy through echocardiography. The patient was advised against competitive sports and started on beta-blockers, preventing potential sudden cardiac arrest.

A 2-year-old from a migrant worker family presented with chronic cough. Dr. Khichar diagnosed foreign body aspiration that had been missed previously. Emergency bronchoscopy removed a small plastic toy piece, with immediate resolution of symptoms and no long-term complications.

A 9-year-old girl with cerebral palsy from a low-income family developed severe scoliosis. Dr. Khichar coordinated with orthopedics for bracing and physical therapy, significantly improving her posture and respiratory function over 8 months without surgical intervention.

A 6-month-old infant presented with failure to thrive and peculiar odors. Dr. Khichar diagnosed phenylketonuria through newborn screening follow-up. Immediate implementation of a special diet prevented intellectual disability, with the family receiving ongoing dietary counseling.

A 14-year-old boy from an upper-middle-class family presented with excessive fatigue. Dr. Khichar diagnosed Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis, a life-threatening condition. Aggressive immunosuppressive therapy led to complete recovery after 6 weeks of hospitalization.

A 4-year-old from a tribal community presented with mysterious skin lesions and joint pain. Dr. Khichar diagnosed Lyme disease, uncommon in their region, and prescribed appropriate antibiotics. Full recovery was achieved within a month, preventing neurological complications.

A 10-year-old diabetic patient was brought in with ketoacidosis. Dr. Khichar stabilized the acute condition and revolutionized their management with continuous glucose monitoring technology, reducing A1c from 12% to 7% in three months through dedicated family education and technology integration.