Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Clinical and pathophysiological concepts of neuralgic amyotrophy.
[neuralgic amyotrophy]
Neuralgic
amyotrophy
--also
known
as
Parsonage-
Turner
syndrome
or
brachial
plexus
neuritis
--
is
a
distinct
and
painful
peripheral
neuropathy
that
causes
episodes
of
multifocal
paresis
and
sensory
loss
in
a
brachial
plexus
distribution
with
concomitant
involvement
of
other
PNS
structures
(
such
as
the
lumbosacral
plexus
or
phrenic
nerve
)
in
a
large
number
of
patients
.
The
phenotype
can
be
limited
or
extensive
and
the
amount
of
disability
experienced
also
varies
between
patients
,
but
many
are
left
with
residual
disabilities
that
affect
their
ability
to
work
and
their
everyday
life
.
Both
idiopathic
and
hereditary
forms
exist
.
The
latter
form
is
genetically
heterogeneous
,
but
in
55
%
of
affected
families
,
neuralgic
amyotrophy
is
associated
with
a
point
mutation
or
duplication
in
the
SEPT
9
gene
on
chromosome
17
q
25
.
The
disease
is
thought
to
result
from
an
underlying
genetic
predisposition
,
a
susceptibility
to
mechanical
injury
of
the
brachial
plexus
(
possibly
representing
disturbance
of
the
epineurial
blood
-nerve
barrier
)
,
and
an
immune
or
autoimmune
trigger
for
the
attacks
.
The
precise
pathophysiological
mechanisms
are
still
unclear
;
treatment
is
empirical
,
and
preventive
measures
are
not
yet
available
.
This
Review
provides
an
overview
of
the
current
clinical
and
pathophysiological
concepts
and
research
topics
in
neuralgic
amyotrophy
.
Diseases
Validation
Diseases presenting
"large number"
symptom
acute rheumatic fever
adrenal incidentaloma
allergic bronchopulmonary aspergillosis
canavan disease
coats disease
cowden syndrome
dedifferentiated liposarcoma
dracunculiasis
epidermolysis bullosa simplex
fabry disease
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
kindler syndrome
legionellosis
malignant atrophic papulosis
neuralgic amyotrophy
phenylketonuria
pleomorphic liposarcoma
primary effusion lymphoma
scrub typhus
severe combined immunodeficiency
triple a syndrome
waldenström macroglobulinemia
well-differentiated liposarcoma
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom