Dr. Nida Pediatric Gastroenterologist & Hepatologist in Indore

Dr. Nida

Pediatric Gastroenterologist & Hepatologist, Indore

MBBS, MD, FNB

  • 9 Years Experience
  • 2 Hospitals

About

After completing MD Pediatrics did two year fellowship in pediatric at Indraprastha Apollo Hospital, New Delhi (by NBE) where specially trained in diseases of child’s digestive system, can perform a number of diagnostic and therapeutic procedures which include: upper and lower endoscopy with biopsies, polypectomies, variceal sclerotherapy and banding, foreign body removal from upper GI tract, dilations, percutaneous liver biopsies .Special interest in inborn and metabolic diseases of children.

Experience

Pediatric gastroenterologist , Indraprastha apollo, New delhi - Currently working here

Specialities

  • Pediatric Gastroenterology & Hepatology

  • Pediatrics

Expertise

Bleeding from the gastrointestinal tract Lactose intolerance Food allergies or intolerances Severe or complicated gastroesophageal reflux disease (reflux or GERD) Inflammatory bowel disease Short bowel syndrome Liver disease Acute or chronic abdominal pain Vomiting Chronic constipation Chronic or severe diarrhea Pancreatic insufficiency (including cystic fibrosis) and pancreatitis Nutritional problems (including malnutrition, failure to thrive, and obesity) Feeding disorders.

Education

MBBS, 2013, MGM Medical College, Indore, India

MD, 2016, JNMCH, Aligarh, India

FNB, 2020, Indraprastha Apollo hospital , Delhi, India

Practice Information

Mohak Hitech Speciality Hospital, Indore

Mohak Hitech Speciality Hospital, Indore

Sri Aurobindo Institute Of Campus, Indore-Ujjain state highway, Near MR-10 crossing, Indore, Madhya Pradesh - 453111

Apollo Hospital, Indore

Apollo Hospital, Indore

Scheme No. 74 C, Sector D, Vijay Nagar, Indore, Madhya Pradesh - 452010

Achievements & Contributions

  • Mirza N, Bharadwaj R, Malhotra S, et alProgressive familial intrahepatic cholestasis type 4 in an Indian child: presentation, initial course and novel compound heterozygous mutationBMJ Case Reports CP 2020;13:e234193
  • A Novel Compound Heterozygous Mutation in ABCB4 Gene Leading to Cholelithiasis, Progressive Familial Intrahepatic Cholestasis (Type 3), and Cirrhosis in a Child November 2020Journal of Child Science DOI: 10.1055/s-0040-1717106
  • Novel Variant ATP8B1 mutation in a child with progressive familial intrahepatic cholestasis (type 1) January 2020Journal of Biochemical and Clinical Genetics DOI: 10.24911/JBCGenetics/183-1581434307
  • Renal Calculi as Initial Presenting Symptom of Glycogen Storage Disease (Type 1 A) in Early Infancy January 2020Journal of Child Science 10(01):e45-e47 DOI: 10.1055/s-0040-1713630
  • Golden aim award 2021
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