Dr. Ankur Kumar Jindal Reviews

A 7-year-old girl from a remote village presented with recurrent high fevers and joint swelling, initially misdiagnosed as common infections. Dr. Jindal identified a rare autoinflammatory syndrome through genetic testing. With targeted biologic therapy, her symptoms resolved completely within 3 months, allowing her to return to school.

A teenage boy from an affluent family with complex multisystem autoimmune disease had failed multiple treatments. Dr. Jindal designed a novel combination therapy using immunomodulators and lifestyle modifications. After 6 months, the patient achieved clinical remission and resumed competitive sports. (Patient of Dr. Kumar)

An adopted 4-year-old with unknown medical history presented with severe skin rashes and developmental delay. Dr. Jindal diagnosed a primary immunodeficiency disorder and initiated immunoglobulin replacement therapy. The child showed remarkable improvement in both health and developmental milestones over 8 months. (Patient of Dr. Kumar)

A 12-year-old from a low-income family with chronic arthritis affecting both knees couldn't afford conventional biologics. Dr. Jindal secured hospital funding for treatment and incorporated physiotherapy. The patient regained full mobility within 4 months and returned to helping his family's agricultural work. (Patient of Dr. Kumar)

A 6-year-old with mysterious recurrent mouth ulcers and abdominal pain was referred after multiple specialist consultations. Dr. Jindal recognized Behçet's disease, rare in children, and started colchicine therapy. Symptoms significantly improved within weeks, with the family learning to manage flare-ups. (Patient of Dr. Kumar)

A newborn from consanguineous parents presented with failure to thrive and recurrent infections. Dr. Jindal diagnosed severe combined immunodeficiency (SCID) and coordinated an emergency bone marrow transplant. The infant recovered fully, with regular follow-ups showing normal immune function development. (Patient of Dr. Kumar)

A 15-year-old athlete developed unexplained muscle weakness and fatigue. Dr. Jindal identified juvenile dermatomyositis through muscle biopsy and initiated corticosteroids and methotrexate. The patient gradually returned to training over 9 months under close monitoring. (Patient of Dr. Kumar)

A 3-year-old refugee child with chronic joint pain and eye inflammation was diagnosed with juvenile idiopathic arthritis-associated uveitis. Dr. Jindal collaborated with ophthalmologists to create a coordinated treatment plan, preventing vision loss and improving mobility. (Patient of Dr. Kumar)

A 10-year-old with periodic fever syndrome had been hospitalized monthly for years. Dr. Jindal prescribed interleukin-1 inhibitors, reducing hospitalizations to once yearly. The patient's academic performance and social life dramatically improved. (Patient of Dr. Kumar)

A 14-year-old girl from a traditional family presented with Raynaud's phenomenon and skin tightening. Dr. Jindal diagnosed juvenile scleroderma early and started aggressive treatment, preventing significant organ involvement and maintaining good quality of life. (Patient of Dr. Kumar)

An 8-year-old with treatment-resistant systemic lupus erythematosus was experiencing kidney involvement. Dr. Jindal implemented cyclophosphamide therapy with careful monitoring, achieving disease control and preserving renal function over 12 months. (Patient of Dr. Kumar)

A 5-year-old with recurrent bone infections was found to have chronic granulomatous disease. Dr. Jindal initiated prophylactic antibiotics and interferon therapy, significantly reducing infection frequency and severity. (Patient of Dr. Kumar)

A 13-year-old boy developed autoimmune encephalitis following a viral infection. Dr. Jindal coordinated with neurologists for immunomodulatory treatment and rehabilitation, resulting in near-complete neurological recovery after 6 months. (Patient of Dr. Kumar)

A 9-year-old with suspected vasculitis presented with purpura and abdominal pain. Dr. Jindal confirmed IgA vasculitis and managed complications through careful medication titration and dietary modifications, achieving full recovery without long-term sequelae. (Patient of Dr. Kumar)

A 2-year-old with failure to thrive and chronic diarrhea was diagnosed with IPEX syndrome. Dr. Jindal arranged for immunosuppressive therapy and nutritional support, stabilizing the child's condition and enabling normal growth trajectory. (Patient of Dr. Kumar)