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Late presentation of congenital diaphragmatic hernia: a case report.
[congenital diaphragmatic hernia]
Delayed
herniation
of
the
abdominal
contents
through
a
congenital
diaphragmatic
hernia
may
occur
beyond
the
neonatal
period
.
This
report
describes
a
9
-
week
-old
female
baby
who
presented
with
excessive
crying
,
irritability
and
respiratory
distress
secondary
to
late
presentation
of
left-sided
congenital
diaphragmatic
hernia
.
The
chest
radiograph
showed
tension
gastrothorax
.
She
underwent
surgical
reduction
of
the
hernia
.
She
made
an
excellent
recovery
and
was
discharged
a
few
days
after
the
operation
.
It
is
assumed
that
sudden
increase
of
the
intra-
abdominal
pressure
caused
herniation
of
abdominal
content
through
a
pre-existing
diaphragmatic
defect
.
This
report
aims
to
increase
the
awareness
of
this
condition
among
physicians
and
pediatric
surgeons
to
allow
early
diagnosis
and
management
.
Diseases
Validation
Diseases presenting
"early diagnosis"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alexander disease
allergic bronchopulmonary aspergillosis
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
coats disease
cohen syndrome
congenital adrenal hyperplasia
congenital diaphragmatic hernia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
cystinuria
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
erdheim-chester disease
erythropoietic protoporphyria
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
hirschsprung disease
holt-oram syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
kabuki syndrome
kallmann syndrome
kindler syndrome
krabbe disease
locked-in syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
triple a syndrome
typhoid
von hippel-lindau disease
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
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