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Central precocious puberty in a 3 year-old girl with Phenylketonuria: a rare association?
[phenylketonuria]
Central
precocious
puberty
(
CPP
)
and
phenylketonuria
(
PKU
)
are
two
rare
conditions
,
the
latter
being
the
rarer
.
To
date
,
only
one
case
featuring
both
these
conditions
has
been
reported
,
and
hyperphenylalaninemia
was
assumed
triggering
CPP
.
We
present
a
3
.
2
 
years
old
girl
referred
with
a
12
 
months
history
of
breast
and
pubic
hair
development
,
and
vaginal
discharge
.
Hyperphenylalaninemia
had
been
identified
by
newborn
screening
and
PKU
subsequently
confirmed
by
plasma
amino
acid
and
genetic
analysis
.
Early
dietary
control
of
plasma
phenylalanine
had
been
excellent
afterwards
,
resulting
in
phenylalanine
concentrations
consistently
within
the
recommended
range
.
Clinical
scenario
,
hormonal
assessment
and
imaging
were
in
keeping
with
true
idiopathic
central
precocious
puberty
.
Treatment
with
long
lasting
gonadotropin-releasing
hormone
analogue
led
to
regression
of
secondary
sexual
characteristics
.
We
describe
for
the
first
time
CPP
in
a
girl
affected
with
PKU
but
with
persistently
well
controlled
blood
phenylalanine
concentrations
.
This
finding
is
in
contrast
to
a
previous
report
which
suggested
persistently
high
phenylalaninemia
levels
as
potential
trigger
for
CPP
in
PKU
patients
.
Our
report
,
together
with
the
lack
of
evidence
in
published
cohort
studies
of
children
with
PKU
,
strongly
suggests
this
rare
association
is
coincidental
and
independent
of
the
presence
of
severe
hyperphenylalaninemia
.
Diseases
Validation
Diseases presenting
"first time"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
congenital adrenal hyperplasia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
gm1 gangliosidosis
harlequin ichthyosis
heparin-induced thrombocytopenia
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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