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[Our experience in the diagnosis of peroxisomal diseases with an abnormal fatty acid profile].
[adrenomyeloneuropathy]
The
aetiology
and
clinical
features
of
peroxisomal
diseases
vary
widely
.
An
altered
very
-
long
-chain
fatty
acid
(
VLCFA
)
profile
is
commonly
found
in
many
of
these
diseases
,
and
this
makes
it
easier
to
point
the
diagnosis
in
the
right
direction
.
We
review
our
experience
in
the
diagnosis
of
cases
of
peroxisomal
diseases
with
an
altered
VLCFA
pattern
;
these
were
determined
in
serum
only
when
there
was
a
strong
clinical
suspicion
up
to
the
end
of
1998
,
when
their
quantification
by
chromatography
was
introduced
into
our
laboratory
.
The
neuropaediatric
database
included
10
,
239
cases
between
May
1990
and
1
st
October
2007
.
Ten
cases
of
peroxisomal
disease
with
an
altered
VLCFA
pattern
were
identified
,
all
of
them
males
.
There
were
two
cases
of
Zellweger
syndrome
spectrum
,
one
unclassified
peroxisomal
oxidation
defect
and
seven
X-
linked
adrenoleukodystrophies
(
four
with
neurological
compromise
and
three
with
no
neurological
damage
;
two
were
identified
in
siblings
of
patients
and
the
other
due
to
the
presence
of
Addison
's
syndrome
)
.
In
our
10
cases
,
the
diagnosis
was
guided
by
the
clinical
or
familial
features
that
led
to
the
determination
of
VLCFA
.
Being
able
to
determine
VLCFA
makes
early
systematic
diagnosis
of
patients
possible
.
At
present
,
VLCFA
determination
is
performed
when
there
is
a
clinical
suspicion
of
Zellweger
spectrum
,
suspected
X-
linked
adrenoleukodystrophy
/
adrenomyeloneuropathy
of
unclear
causation
,
Addison
's
disease
,
both
in
males
and
females
,
and
above
all
in
cases
of
chronic
encephalopathy
of
unknown
causation
,
with
or
without
prenatal
onset
.
Diseases
Validation
Diseases presenting
"prenatal onset"
symptom
adrenomyeloneuropathy
dentinogenesis imperfecta
monosomy 21
zellweger syndrome
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