Karunesh Kumar

About

MD, FNB (PGHN), RCPCH Fellowship (GOSH, LOndon, UK), RCPCH Fellowship (King's College, London, UK)
Consultant
Pediatric Gastroenterologist, Hepatologist and Nutritionist
Indraprastha Apollo Hospitals, New Delhi

Key interest areas:
GI -
Nutritional rehabilitation and neurogastroenterology
Persistent and chronic diarrhea

Liver -
Neonatal cholestatsis
Metabolic and genetic disorders
Transplantation out come and long term follow up of liver trans[plant recipients.

Pancreas-
Chronic pancreatitis and exocrine pancreatic insufficiency

Employment

• Indraprastha Apollo Hospitals Consultant
  2020 - Present

Education

• Great Ormond Street Hospital for Children NHS Foundation Trust RCPCH Fellow
  2019 - 2020
• Indraprastha Apollo Hospital FNB
  2014 - 2016
• Maulana Azad Medical College MD
  2009 - 2012

Projects & Funding

Projects & funding information is unavailable.

Publications (30)

• Primary versus Post-Kasai Liver Transplantation for Biliary Atresia in Children: A Comparative Living Donor Transplant Experience.
  Journal of Clinical and Experimental Hepatology 2026 DOI: 10.1016/j.jceh.2026.103640
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• Peri-anal Hyperpigmentation in a Patient with Rectal Cavernous Haemangioma
  Apollo Medicine 2025 DOI: 10.1177/09760016241310280
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• DOCK11 deficiency-related immune dysregulation leading to paediatric acute liver failure
  BMJ Case Reports 2025 DOI: 10.1136/bcr-2024-263427
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• Management of Acute Liver Failure in Children
  Apollo Medicine 2024 DOI: 10.1177/09760016241299530
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• Colorectal Polyps in Tuberous Sclerosis– A Rare Occurrence in Pediatrics
  Indian Journal of Pediatrics 2024 DOI: 10.1007/s12098-024-05303-x
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• Diagnosis and management of pediatric acute liver failure: consensus recommendations of the Indian Society of Pediatric Gastroenterology, Hepatology, and Nutrition (ISPGHAN)
  Hepatology International 2024 DOI: 10.1007/s12072-024-10720-3
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• Fever Triggered Recurrent Acute Liver Failure due to RINT1 Deficiency
  Indian Journal of Pediatrics 2024 DOI: 10.1007/s12098-024-05230-x
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• Genotype correlates with clinical course and outcome of children with tight junction protein 2 (TJP2) deficiency-related cholestasis
  Hepatology 2024 DOI: 10.1097/HEP.0000000000000828
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• Hepatoblastoma in a cirrhotic child with Alagille syndrome
  BMJ Case Reports 2024 DOI: 10.1136/bcr-2022-253080
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• Natural course and outcomes of children with ubiquitin-specific protease 53 (USP53)-related genetic chronic cholestasis
  Journal of Pediatric Gastroenterology and Nutrition 2024 DOI: 10.1002/jpn3.12392
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