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Progression of cerebral white matter abnormalities in early treated patients with phenylketonuria during adolescence.
[classical phenylketonuria]
In
this
study
of
cranial
MRI
a
group
of
15
adolescents
with
classical
phenylketonuria
and
permanent
blood
phenylalanine
(
phe
)
checks
from
infancy
was
investigated
twice
with
an
interval
of
three
years
in
between
.
Cranial
MRI
revealed
a
progression
of
white
matter
abnormalities
in
patients
with
moderate
and
poor
control
of
blood
phe
levels
,
however
not
in
well
controlled
patients
.
Nevertheless
results
indicate
an
individual
vulnerability
of
the
brain
against
elevated
phenylalanine
levels
in
phenylketonurics
.
Diseases
Validation
Diseases presenting
"blood phe levels"
symptom
classical phenylketonuria
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