Work Statics:

Hospital has in-house 24*7 laboratory, histopathology lab, immunology lab, radiology services, provision for real-time US guided Kidney biopsy, in house CT scan, Radionuclide scan facilities, urodynamics and actively running interventional radiology department.

State-of-art-treatment facilities available at par with international standards and recommendations:

• Low Density Lipoprotein- Apheresis (LDL-A) is indicated in children with Multi-Drug Resistant Nephrotic Syndrome. IKDRC-ITS is the first center in India successfully offering LDL-A as a therapeutic modality for multi-drug resistant nephrotic syndrome.
  
  

  No of children who received LDL-A treatment	11
  Compete response	07
  Partial remission	01
  No response	02
  Death	01



• Hereditary Tyrosinemia Type 1 is an inherited disorder with autosomal recessive inheritance that affects primarily the liver and kidney. It’s treatment has been revolutionized by Nitisinone, eliminating the need for liver transplantation eventually required when chronic liver disease develops. Now this breakthrough treatment is available at IKDRC pharmacy.
  
  

  	2023	2024	2025(till July 2025)
  No. of children diagnosed with HT- type 1	06	08	4
  No. of children on treatment with Nitisinone	05	11	15
  No. of children who expired	01 Before Nitisinone was made available	1 Due to disease progression	0



• Nephropathic Cystinosis is an autosomal recessive inherited genetic disorder where amino acid cystine accumulates in the body cells and tissues including Fanconi syndrome in the kidneys. Early diagnosis and treatment with cysteamine are critical to manage these children and delay progression to end stage kidney failure.
  
  

  	2024	2025(till July 2025)
  Total no. of children diagnosed with cystinosis	08	10
  No. of children on cysteamine	08	09
  No. of newly diagnosed cases	03	02
  No. of children with cystinosis on dialysis	00	00
  Received transplant	02	02
  Lost to follow up	00	01



• Nephrogenetics is the study of genetic basis of kidney diseases. It encompasses how genetic variations influence the development, function, and susceptibility to kidney disorders. The well-equipped genetic laboratory at IKDRC-ITS enables the accurate diagnosis of various inherited conditions in children with kidney diseases enabling proper prognosis, appropriate treatment as well as familial screening and prenatal counselling.
  
  

  Suspected Phenotypes	Till 2023	2024
  Nephrotic syndrome	120	28
  Cystic kidney disease	56	10
  Kidney stone work up	52	11
  Tubulopathy	45	07
  other	27	29+ 22 reports pending
  Lost to follow up	00	01