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Spontaneous reattachment of a posteriorly dislocated endothelial graft: a case report.
[aniridia]
A
thirty
-
year
-old
Chinese
man
with
a
history
of
severe
trauma
to
his
right
eye
,
with
secondary
sectoral
aniridia
and
multiple
operations
including
intraocular
lens
insertion
more
than
fifteen
years
ago
,
underwent
an
uneventful
Descemet
's
Stripping
Automated
Endothelial
Keratoplasty
(
DSAEK
)
for
his
pseudophakic
bullous
keratopathy
in
a
tertiary
hospital
in
Hong
Kong
.
The
nature
of
his
previous
operations
was
unknown
to
the
surgeon
at
the
time
of
transplant
.
On
postoperative
day
one
,
the
graft
was
not
present
in
the
anterior
chamber
.
Fundal
view
was
limited
because
of
corneal
oedema
.
B-
scan
ultrasonography
could
not
detect
any
definite
presence
of
a
donor
button
in
the
posterior
segment
as
gas
was
present
in
the
vitreous
cavity
.
The
patient
was
instructed
to
lie
prone
full
time
,
and
on
postoperative
day
three
,
the
graft
was
found
to
be
reattached
to
the
stroma
with
spontaneous
resolution
of
corneal
oedema
,
indicating
restoration
of
pump
function
of
endothelium
graft
.
This
is
the
first
case
of
spontaneous
reattachment
of
a
posteriorly
dislocated
endothelial
graft
without
surgical
intervention
or
abandonment
of
the
grafted
endothelial
button
.
Diseases
Validation
Diseases presenting
"first case"
symptom
achondroplasia
adrenal incidentaloma
allergic bronchopulmonary aspergillosis
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
child syndrome
cholangiocarcinoma
classical phenylketonuria
coats disease
cohen syndrome
congenital toxoplasmosis
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
esophageal adenocarcinoma
esophageal carcinoma
fabry disease
familial mediterranean fever
focal myositis
gm1 gangliosidosis
harlequin ichthyosis
hodgkin lymphoma, classical
homocystinuria without methylmalonic aciduria
junctional epidermolysis bullosa
kabuki syndrome
krabbe disease
lamellar ichthyosis
legionellosis
liposarcoma
locked-in syndrome
malignant atrophic papulosis
monosomy 21
neonatal adrenoleukodystrophy
oculocutaneous albinism
omenn syndrome
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
systemic capillary leak syndrome
thoracic outlet syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
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