Tag: Inherited diseases

Statistics show that secondary immunodeficiencies are far more common than primary immunodeficiencies, with the distinction often determined by the root cause. The core difference between primary and secondary deficiencies lies in their origin: one is an inherited genetic condition, while the other is acquired later in life due to an external factor.

The human body requires 20 different amino acids to function, yet it can only produce 11 of them, making the remaining nine essential and crucial to obtain from the diet. This leads to the question: **What is the disease associated with essential amino acids?** The answer encompasses both genetic disorders affecting metabolism and acquired nutritional deficiencies.

Genetic mutations can impair the body’s ability to properly metabolize lysine, leading to a cluster of inherited metabolic disorders. Understanding **what are the diseases associated with lysine** is crucial, as they can range from benign conditions to severe neurological disorders affecting growth and development.