Rare Diseases Symptoms Automatic Extraction
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Diagnosing and managing hip problems in childhood.
[pyomyositis]
The
hip
and
proximate
tissues
are
implicated
in
a
variety
of
childhood
conditions
,
and
in
the
differential
diagnosis
of
many
more
.
To
a
large
extent
the
possible
diagnoses
are
limited
by
the
child
's
age
,
an
accurate
history
and
thorough
examination
.
Developmental
dysplasia
of
the
hip
(
DDH
)
is
a
spectrum
disorder
of
joint
development
and
/
or
instability
.
It
is
a
major
cause
of
morbidity
in
children
and
adults
.
It
can
be
classified
into
three
types
:
neuromuscular
;
teratological
;
and
idiopathic
(
the
most
common
type
)
.
Examination
of
the
hips
is
carried
out
neonatally
using
Ortolani
and
Barlow
manoeuvres
to
look
for
dislocation
.
These
tests
have
high
sensitivity
but
low
specificity
,
and
this
is
one
reason
why
DDH
is
still
picked
up
late
.
When
a
limping
child
presents
it
is
important
that
the
less
common
diagnoses
,
including
infection
,
neoplasia
and
slipped
femoral
epiphysis
are
kept
in
mind
and
urgent
referral
made
if
necessary
.
In
one
study
,
where
a
diagnosis
was
made
,
the
hip
joint
was
the
culprit
in
the
majority
of
cases
.
Of
these
,
40
%
were
diagnosed
as
irritable
hip
or
transient
synovitis
.
Other
inflammatory
arthritides
/
tendinoses
accounted
for
3
.
2
%
,
Perthes
'
disease
2
%
,
and
infection
3
.
6
%
.
Any
age
group
is
vulnerable
to
infection
such
as
septic
arthritis
,
osteomyelitis
and
pelvic
pyomyositis
.
Early
diagnosis
and
treatment
,
comprising
antibiotics
with
or
without
surgery
,
is
critical
.
In
the
limping
child
,
fever
with
focal
tenderness
or
restricted
range
of
movement
is
indicative
of
infection
unless
investigations
show
otherwise
.
Diseases
Validation
Diseases presenting
"fever"
symptom
22q11.2 deletion syndrome
acute rheumatic fever
alexander disease
allergic bronchopulmonary aspergillosis
canavan disease
carcinoma of the gallbladder
child syndrome
congenital toxoplasmosis
cushing syndrome
cystinuria
dracunculiasis
erdheim-chester disease
esophageal adenocarcinoma
esophageal carcinoma
familial mediterranean fever
focal myositis
hodgkin lymphoma, classical
lamellar ichthyosis
legionellosis
locked-in syndrome
malignant atrophic papulosis
neonatal adrenoleukodystrophy
neuralgic amyotrophy
oculocutaneous albinism
papillon-lefèvre syndrome
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
typhoid
waldenström macroglobulinemia
wolf-hirschhorn syndrome
This symptom has already been validated