Umbilical cord blood gas analysis provides valuable insights into fetal oxygenation and acid-base balance during labor and...
amit2k8pmch
Recurrent episodes of symptomatic hypoglycemia in a 2-year-old child warrant a structured and systematic diagnostic approach. Hypoglycemia...
“Powerful Pediatric Diet Plans for Metabolic Disorders: Top Nutritional Strategies” IntroductionMetabolic disorders in children require specialized care,...
Newborn screening is a critical healthcare practice aimed at identifying certain genetic, metabolic, and endocrine disorders in...
Inborn Errors of Metabolism (IEM) IEM are rare genetic disorders affecting the body’s metabolic pathways. Timely diagnosis...
Introduction Infantile Polycystic Kidney Disease (PKD) is a rare genetic disorder that can have life-altering implications. In...
FANCONI SYNDROME Fanconi syndrome is a rare condition involving proximal tubule dysfunction, leading to multiple biochemical abnormalities....
What is Bartter Syndrome? Bartter Syndrome is a rare inherited kidney disorder affecting the body’s ability to...
What is the Pediatric RIFLE Criteria? The Pediatric RIFLE (pRIFLE) criteria classify the severity of acute kidney...
What is Renal Osteodystrophy? Renal osteodystrophy is a bone disorder associated with chronic kidney disease (CKD). It...
