Neonatal jaundice is a common condition in newborns causing yellowing of the skin and eyes due to excess bilirubin in the blood. It can be caused by various factors, including immature liver function and certain medical conditions. While often harmless, severe cases can lead to complications.
Jaundice (Hyperbilirubinemia)
Jaundice, a condition characterized by yellowing of the skin and eyes, is caused by hyperbilirubinemia, an abnormally high level of bilirubin in the blood. It can be a symptom of various liver or biliary tract diseases.
Thalassemia
Thalassemia is an inherited blood disorder causing reduced hemoglobin production. Symptoms include fatigue, weakness, and jaundice. Treatment involves blood transfusions, iron chelation, and bone marrow transplants.

Essentials of Folate Blood Test
A folate blood test measures the amount of folate in your blood. Folate is crucial for pregnancy health and overall well-being. Schedule your test today.

Lead Poisoning
Lead poisoning is preventable. Learn about risks in homes, water, and toys. Find out how to test and reduce exposure.

Homocysteine & Hyperhomocysteinemia
Homocysteine is an amino acid linked to an increased risk of heart disease. Elevated levels can be influenced by genetics, diet, and lifestyle.
Sickle Cell Test
This test unmasks sickle cells: crescent shadows under the microscope, revealing HbS’s hidden grip on red blood cells.
Hemolysate Preparation for Hb Electrophoresis or Alkaline Denaturation Tests
Red blood cells lysed to release hemoglobin for Hb electrophoresis and alkaline denaturation test. Hemolysate preparation requires careful steps to ensure accuracy and reliability of results.
Alpha Thalassemia
Alpha thalassemia is an inherited blood disorder that causes less alpha globin production, leading to less hemoglobin formation thus resulting in anemia.
High Performance Liquid Chromatography (HPLC) for Identification of Hemoglobin Subtypes
HPLC for hemoglobin subtype identification separates and quantifies different hemoglobin variants based on their unique chromatographic properties.
Glucose-6-Phosphate Dehydrogenase (G6PD) Fluorescent Spot Test
The G6PD fluorescent spot test is a rapid and simple screening method for G6PD deficiency that utilizes the enzyme’s ability to reduce NADP+ to NADPH.
Anemia: Types, Symptoms & Treatment
Anemia is a condition characterized by a deficiency in red blood cells or hemoglobin below the physiological need of the body.