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New insights in growth of phenylketonuric patients.
[phenylketonuria]
Treatment
of
phenylketonuria
involves
a
restriction
in
the
intake
of
natural
proteins
.
This
can
lead
to
growth
impairment
.
Weight
,
height
and
body
mass
index
of
109
hyperphenylalaninemic
patients
(
mild
hyperphenylalaninemia
(
HPA
)
and
phenylketonuria
(
PKU
)
)
were
determined
from
birth
until
18
Â
years
,
every
6
Â
months
,
and
differences
to
the
healthy
population
,
depending
on
the
age
,
sex
and
phenotype
,
were
analyzed
.
Data
collection
was
longitudinal
retrospective
during
31
Â
years
.
Statistical
analysis
of
z-score
values
was
performed
by
advanced
statistical
tools
.
Long
-term
evolution
of
anthropometric
z-scores
showed
no
significant
statistical
differences
between
PKU
and
mild
HPA
individuals
,
according
to
the
general
population
.
For
PKU
individuals
,
height
is
slightly
lower
and
weight
slightly
higher
than
in
the
healthy
population
,
but
differences
are
smaller
than
one
standard
deviation
.
Nevertheless
,
over-time
evolutions
of
female
height
z-scores
are
different
in
each
type
of
pathology
,
with
a
crossover
between
8
and
12
Â
years
(
p
 
=
 
0
.
0186
)
.
Conclusions
:
It
is
nowadays
possible
to
achieve
a
long
-term
normal
growth
in
PKU
patients
with
appropriate
dietary
treatment
.
There
is
however
an
acceleration
of
growth
up
to
8
Â
years
old
for
PKU
female
patients
that
leads
to
a
slightly
lower
final
height
.
Detection
of
this
behaviour
was
possible
by
using
nonlinear
mixed
effects
models
.
Diseases
Validation
Diseases presenting
"female patients"
symptom
adrenomyeloneuropathy
aromatase deficiency
benign recurrent intrahepatic cholestasis
carcinoma of the gallbladder
classical phenylketonuria
congenital adrenal hyperplasia
cushing syndrome
erdheim-chester disease
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial hypocalciuric hypercalcemia
familial mediterranean fever
heparin-induced thrombocytopenia
lymphangioleiomyomatosis
oligodontia
papillon-lefèvre syndrome
phenylketonuria
pyruvate dehydrogenase deficiency
sneddon syndrome
trochlear dysplasia
von hippel-lindau disease
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
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