Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Fabry disease.
[fabry disease]
Fabry
disease
(
FD
)
is
an
X-
linked
disorder
caused
by
deficiency
of
the
enzyme
alpha-galactosidase
A
,
required
for
the
degradation
of
globotriaosylceramide
.
Accumulation
of
substrate
occurs
in
multiple
cell
types
resulting
in
a
multi-system
disorder
,
affecting
both
males
and
females
.
Clinical
features
include
neuropathic
pain
and
angiokeratoma
,
with
subsequent
development
of
proteinuria
,
renal
failure
,
left
ventricular
hypertrophy
,
arrhythmias
and
stroke
.
Beyond
palliative
therapies
for
organ
involvement
and
pain
control
,
enzyme
replacement
therapy
directed
at
the
underlying
metabolic
defect
became
available
in
2001
-
2003
.
Knowledge
of
the
pathophysiology
and
clinical
features
of
FD
is
vital
for
assessing
the
rationale
and
evidence
of
efficacy
of
therapies
for
FD
and
their
limitations
.
Whilst
ERT
improves
many
of
the
symptoms
of
FD
,
its
effect
on
the
natural
history
of
the
disorder
has
yet
to
be
fully
demonstrated
.
Improved
understanding
of
the
appropriate
use
of
adjunctive
therapies
and
the
development
of
new
treatment
strategies
,
including
pharmacologic
chaperone
therapy
and
gene
therapy
,
coupled
with
long
term
clinical
outcome
data
on
the
effects
of
ERT
are
all
key
components
of
optimising
treatment
for
FD
.
Diseases
Validation
Diseases presenting
"pain"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
aniridia
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital diaphragmatic hernia
congenital toxoplasmosis
cushing syndrome
cutaneous mastocytosis
cystinuria
dedifferentiated liposarcoma
dentin dysplasia
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
focal myositis
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
junctional epidermolysis bullosa
kabuki syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
neuralgic amyotrophy
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
phenylketonuria
pleomorphic liposarcoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
scrub typhus
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
trochlear dysplasia
typhoid
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
wolf-hirschhorn syndrome
This symptom has already been validated