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Amino Acid Protein Chemistry
Amino AcidTo be able to write the amino acid, the C-H should be in the center, and they should get attached to CORN (CO is the Carboxyl group, R
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Sep 26 2024
Amino Acid Protein Chemistry
Glycogen Storage Diseases
Glycogen storage diseases are inherited conditions in which there is an inability of the body to store and metabolize glycogen efficiently leadin...
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Apr 16 2024
Glycogen Storage Diseases
Fanconi Anemia: Symptoms, Causes and Treatment
Fanconi anemia is an autosomal recessive disease ( Inheritance) characterized by bone marrow failure leading to pancytopenia. It is one of the ca...
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Mar 29 2024
Fanconi Anemia: Symptoms, Causes and Treatment
Phenylketonuria: Symptoms, Causes and Treatment
PKU, sometimes called phenylketonuria, is a rare genetic disorder that causes the body to accumulate the amino acid phenylalanine. PKU is caused
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Mar 20 2024
Phenylketonuria: Symptoms, Causes and Treatment
MCAD Deficiency: Causes, Symptoms, Risk Factors, Diagnosis, Treatment and Complications
Medium chain acyl-coenzyme Your body cannot turn certain fats into energy due to a genetic disorder known as a dehydrogenase (MCAD) deficiency. M...
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Jan 08 2024
MCAD Deficiency: Causes, Symptoms, Risk Factors, Diagnosis, Treatment and Complications
Gaucher Disease: Causes, Symptoms, Risk Factors, Diagnosis
Gaucher disease can result from an accumulation of particular fatty substances in particular organs, primarily the liver and spleen. This causes
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Dec 26 2023
Gaucher Disease: Causes, Symptoms, Risk Factors, Diagnosis