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Therapy of X-linked adrenoleukodystrophy.
[adrenomyeloneuropathy]
X-
linked
adrenoleukodystrophy
(
X-
ALD
;
OMIM
#
300100
)
is
caused
by
defects
of
the
ABCD
1
gene
on
chromosome
Xq
28
,
resulting
in
an
impairment
of
peroxisomal
beta
-oxidation
and
the
accumulation
of
saturated
very
long
chain
fatty
acids
(
VLCFAs
)
.
Primary
manifestations
occur
in
the
CNS
,
the
adrenal
cortex
and
the
testes
'
Leydig
cells
.
The
clinical
presentation
shows
a
marked
variability
which
is
not
explained
by
the
different
X-
ALD
genotypes
.
Phenotypes
range
from
rapidly
progressive
cerebral
disease
with
childhood
(
childhood
cerebral
ALD
[
CCALD
]
)
or
adulthood
(
adult
cerebral
ALD
[
ACALD
]
)
onset
leading
to
death
within
a
few
years
,
over
adult-onset
adrenomyeloneuropathy
(
AMN
)
with
or
without
focal
CNS
demyelination
,
AMN
converting
into
a
rapidly
progressive
,
cerebral
demyelinating
phenotype
resembling
CCALD
,
to
slow
disease
progression
over
decades
,
or
adrenal
insufficiency
only
.
Approximately
50
%
of
female
heterozygotes
develop
moderate
spastic
paresis
resembling
the
AMN
phenotype
.
This
review
focuses
on
current
experiences
with
different
therapeutic
approaches
.
Lorenzo
's
oil
did
not
prove
to
be
effective
in
cerebral
inflammatory
disease
variants
,
but
asymptomatic
patients
,
and
speculatively
AMN
variants
without
cerebral
involvement
,
as
well
as
female
carriers
may
benefit
from
early
intake
of
oleic
and
erucic
acids
in
addition
to
VLCFA
restriction
.
Hormone-replacement
therapy
is
necessary
in
all
patients
with
adrenal
insufficiency
.
Hematopoietic
stem
cell
transplantation
has
been
reported
to
be
effective
in
presymptomatic
or
early
symptomatic
CCALD
,
and
may
well
also
be
a
final
therapeutic
option
in
early
ACALD
patients
.
Early
detection
of
mutation
carriers
and
timely
initiation
of
therapy
is
important
for
the
effectiveness
of
all
therapeutic
efforts
.
Gene
therapy
of
endogenous
hematopoietic
stem
cells
,
pharmacological
upregulation
of
other
genes
encoding
proteins
involved
in
peroxisomal
beta
-oxidation
,
reduction
of
oxidative
stress
,
and
possibly
lovastatin
are
candidates
for
future
X-
ALD
therapies
.
Diseases
Validation
Diseases presenting
"very long chain fatty acids"
symptom
adrenomyeloneuropathy
gm1 gangliosidosis
krabbe disease
lamellar ichthyosis
neonatal adrenoleukodystrophy
pyruvate dehydrogenase deficiency
triple a syndrome
von hippel-lindau disease
x-linked adrenoleukodystrophy
zellweger syndrome
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