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Phenylketonuria শব্দের বাংলা অর্থ: ফিনাইলকিটোনিউরিয়াল
Phenylketonuria Meaning In Bengali ফিনাইলকিটোনিউরিয়াল
Phenylketonuria
Definition
1) Phenylketonuria, also known as PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to build up to toxic levels in the body. This can lead to intellectual disabilities, developmental delays, and other health problems if not treated.
2) Phenylketonuria is a metabolic disorder characterized by the body's inability to process phenylalanine properly. This results in high levels of phenylalanine in the blood, which can be harmful to the brain and nervous system.
3) Phenylketonuria is typically diagnosed through newborn screening tests, and treatment usually involves following a strict low-phenylalanine diet to prevent complications associated with the condition.
Examples
Phenylketonuria Example in a sentence
1) Phenylketonuria is a genetic disorder that affects the body's ability to break down a specific amino acid.
2) Infants with phenylketonuria need to follow a restricted diet to prevent complications.
3) If left untreated, phenylketonuria can lead to intellectual disabilities.
4) Blood tests are commonly used to screen for phenylketonuria in newborns.
5) Phenylketonuria is managed by avoiding foods high in phenylalanine.
6) People with phenylketonuria must diligently monitor their diet for life.
7) The severity of phenylketonuria can vary from person to person.
8) Phenylketonuria can be diagnosed through genetic testing.
9) Early detection and treatment of phenylketonuria are crucial for preventing complications.
10) Parents of children with phenylketonuria often work closely with healthcare providers to manage the condition effectively.
Part of Speech
Phenylketonuria (Noun)
Synonyms
Encyclopedia
Phenylketonuria, also known as PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to build up to toxic levels in the body. This can lead to intellectual disabilities, developmental delays, and other health problems if not treated.
Phenylketonuria is a metabolic disorder characterized by the body's inability to process phenylalanine properly. This results in high levels of phenylalanine in the blood, which can be harmful to the brain and nervous system.
Phenylketonuria is typically diagnosed through newborn screening tests, and treatment usually involves following a strict low-phenylalanine diet to prevent complications associated with the condition.
