tyrosinemia Antonyms
No Synonyms and anytonyms found
Meaning of tyrosinemia
Wordnet
tyrosinemia (n)
autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation
tyrosinemia Sentence Examples
- Tyrosinemia is a rare metabolic disorder characterized by an inability to properly break down tyrosine, an amino acid.
- Neonatal tyrosinemia is the most severe form of tyrosinemia, presenting with liver failure within the first few days of life.
- Type I tyrosinemia is caused by a deficiency of the fumarylacetoacetate hydrolase (FAH) enzyme.
- Type II tyrosinemia is caused by a deficiency of the tyrosine aminotransferase (TAT) enzyme.
- Type III tyrosinemia is caused by a deficiency of the 4-hydroxyphenylpyruvate dioxygenase (HPPD) enzyme.
- Symptoms of tyrosinemia can include vomiting, liver damage, intellectual disability, and skin problems.
- Treatment for tyrosinemia typically involves a low-tyrosine diet and medications to reduce tyrosine levels.
- Liver transplantation may be necessary in severe cases of tyrosinemia.
- Genetic testing can be used to diagnose tyrosinemia and identify the specific enzyme deficiency causing the condition.
- Advances in medical research have improved the outlook for individuals with tyrosinemia, but early diagnosis and treatment are essential.
FAQs About the word tyrosinemia
autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation
No synonyms found.
No antonyms found.
Tyrosinemia is a rare metabolic disorder characterized by an inability to properly break down tyrosine, an amino acid.
Neonatal tyrosinemia is the most severe form of tyrosinemia, presenting with liver failure within the first few days of life.
Type I tyrosinemia is caused by a deficiency of the fumarylacetoacetate hydrolase (FAH) enzyme.
Type II tyrosinemia is caused by a deficiency of the tyrosine aminotransferase (TAT) enzyme.
