inborn error of metabolism

It is a common inborn error of metabolism among humans.

It is caused by an inherited inborn error of metabolism.

However, in Japan, it is the single most prevalent inborn error of metabolism.

For more online resources and references, see inborn error of metabolism.

When cases occur now, doctors are urged to look for a genetic disorder known as an inborn error of metabolism.

Also, some inborn errors of metabolism are associated with autism, but probably account for less than 5% of cases.

A congenital metabolic disease is also referred to as an inborn error of metabolism.

Livers have been transplanted as single organs for at least 16 inborn errors of metabolism.

Leukotriene C4 synthase deficiency is an inborn error of metabolism.

Scriver made many important contributions to our knowledge of inborn errors of metabolism.

The genetic defect, an inborn error of metabolism, causes people to absorb too much iron from the diet.

It is an inborn error of metabolism, and one of the lysosomal storage diseases.

Urea cycle disorders are included in the category of inborn errors of metabolism.

His seminal text, Inborn Errors of Metabolism was published in 1923.

It is one of several inborn errors of metabolism included in the Garrod's tetrad.

Inborn errors of metabolism such as Fructose malabsorption.

Each represents an inherited inborn error of metabolism involving the amino acid, proline.

Galactokinase deficiency is one of the three inborn errors of metabolism that lead to hypergalactosemia.

His research into methods for screening inborn errors of metabolism has led to the investigation and reporting, with co-workers, of numerous cases.

Human fetal tissue has already been used to treat disorders ranging from inborn errors of metabolism to neurodegenerative diseases for all age groups.

Archibald Garrod and the development of the concept of inborn errors of metabolism.

These tests might evaluate for chromosomal disorders, inborn errors of metabolism, or single gene disorders.

People with certain rare inborn errors of metabolism have a propensity to accumulate crystal-forming substances in their urine.

These tests can find dozens of congenital metabolic diseases (also known as Inborn error of metabolism).

It is an inborn error of metabolism characterized by a deficiency of the enzyme steroid sulfatase.