-
Phenylketonuria (PKU) is an
inborn error of
metabolism that
results in
decreased metabolism of the
amino acid phenylalanine.
Untreated PKU can lead to...
- is
biosynthesized via the
shikimate pathway. The
genetic disorder phenylketonuria (PKU) is the
inability to
metabolize phenylalanine because of a lack...
- The
European Society for
Phenylketonuria and
Allied Disorders Treated as
Phenylketonuria (E.S.PKU) is a Europe-based non-profit organization. It was founded...
- be
screened for
phenylketonuria and hypothyroidism,
among other congenital disorders. Hypothesis: "The
newborns have
phenylketonuria and hypothyroidism"...
- malaria. Such
disorders include cystic fibrosis,
sickle cell disease,
phenylketonuria and thal****aemia.
Hereditary defects in
enzymes are
generally inherited...
- n-3 long-chain
polyunsaturated fatty acid
values in
patients with
phenylketonuria: a
systematic review and meta-analysis".
Nutrition Research. 33 (7):...
- diseases,
including GLUT1
deficiency syndrome, Lesch–Nyhan syndrome,
phenylketonuria, and
Huntington disease and can be a
feature of
kernicterus (rapidly...
- the
other is a rare or even
novel one.[citation needed]
Phenylketonuria.
Because phenylketonuria was the
first genetic disorder for
which m**** post-natal...
-
synthase (PTPS) deficiency. Also, BH4*2HCL is FDA
approved for use in
phenylketonuria (PKU),
along with
dietary measures. However, most
people with PKU have...
- development. Medium-chain acyl-coenzyme A
dehydrogenase deficiency (MCADD)
Phenylketonuria, a
disorder where an
error in
amino acid
metabolism can
impair brain...
