Examples of using Inborn error in English and their translations into Portuguese
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Kolbam is used to treat these‘inborn errors of bile acid synthesis.
No data regarding cholic acid treatment are available in patients with inborn errors of bile acid metabolism with hepatic impairment unrelated to their primary disease.
Both deficiencies are considered inborn errors of metabolism that cause mental deficits when diagnosis
Ch due to dyshormonogenesis is a disease caused by inborn errors in t3 and t4 synthesis, with autosomal recessive inheritance.
Inborn errors of primary bile acid synthesis involve congenital defects in the primary enzymes responsible for catalysing key reactions in the synthesis of cholic and chenodeoxycholic acids.
Mucopolysaccharidoses(mps) are inborn errors of metabolism and belong to the group of lysosomal storage diseases.
Specialty genetics clinics focusing on management of inborn errors of metabolism, skeletal dysplasia,
Inborn errors of metabolism were not included in the diagnoses because they had already been identified by universal neonatal screening.
Exome sequencing effectively identifies inborn errors of metabolism," agrees neurologist Fernando Kok,
The inborn errors of metabolism represent a heterogeneous category of genetic diseases caused by enzyme deficiencies.
safety of cholic acid treatment in patients with inborn errors of bile acid metabolism was evaluated.
Ammonia serum concentration is commonly raised in liver diseases and in inborn errors of urea cycle.
obesity and inborn errors of metabolism.
Treatment with exogenous cholic acid is intended to replace physiological bile acid in cases of inborn errors of bile acid synthesis.
congenital malformation and inborn errors of metabolism.
malnutrition and inborn errors of metabolism.
They are a part of a group of hereditary metabolic diseases known as inborn errors of metabolism.
does it include inborn errors of metabolism.
Specifically in the neonatal period, inborn errors of cobalamin metabolism due to alterations in the MMACHC gene responsible for the production of factor cobalamin-b Clc-b,
particularly inborn errors of metabolism, the mechanism of disease is well understood