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Phenylketonuria with acute myeloblastic leukemia in a 9-year-old boy: reporting a rare case.
[classical phenylketonuria]
Phenylketonuria
is
a
genetic
metabolic
disorder
resulting
in
phenylalanine
accumulation
in
blood
.
Phenylacetate
,
which
is
an
abnormal
phenylalanine
metabolities
,
was
hypothesized
to
have
anticancer
activity
.
Two
-
years
-old
boy
was
diagnosed
with
classical
phenylketonuria
because
of
mental
motor
retardation
.
When
the
patient
was
9
-
year
-old
,
he
developed
acute
myeloblastic
leukemia
.
Here
,
we
present
the
case
with
phenylketonuria
and
acute
myeloblastic
leukemia
because
of
its
extreme
rarity
.
Diseases
Validation
Diseases presenting
"was hypothesized to have anticancer activity"
symptom
classical phenylketonuria
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