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Parenteral nutrition in patients with inborn errors of metabolism - a therapeutic problem.
[phenylketonuria]
Parenteral
nutrition
is
now
a
standard
part
of
supportive
treatment
in
pediatric
departments
.
We
describe
four
cases
in
which
parenteral
nutrition
was
extremely
difficult
due
to
coincidence
with
inborn
errors
of
metabolism
.
The
first
two
cases
was
fatty
acid
beta
-oxidation
disorders
associated
with
necrotizing
enterocolitis
and
congenital
heart
disease
.
Thus
,
limitations
of
intravenous
lipid
intake
made
it
difficult
to
maintain
a
good
nutritional
status
.
The
third
case
was
phenylketonuria
associated
with
a
facial
region
tumour
(
rhabdomyosarcoma
)
,
in
which
parenteral
nutrition
was
complicated
because
of
a
high
phenylalanine
content
in
the
amino
acid
formulas
for
parenteral
nutrition
.
The
fourth
patient
was
a
child
with
late
-diagnosed
tyrosinemia
type
1
,
complicated
with
encephalopathy
-
during
intensive
care
treatment
the
patient
needed
nutritional
support
,
including
parenteral
nutrition
-
we
observed
amino
acid
formula
problems
similar
to
those
in
the
phenylketonuria
patient
.
Parenteral
nutrition
in
children
with
inborn
errors
of
metabolism
is
a
rare
,
but
very
important
therapeutic
problem
.
Total
parenteral
nutrition
formulas
are
not
prepared
for
this
group
of
diseases
.
Diseases
Validation
Diseases presenting
"very important therapeutic problem"
symptom
phenylketonuria
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