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Successful renal transplant in a patient with non-Herlitz junctional epidermolysis bullosa.
[junctional epidermolysis bullosa]
Non-
Herlitz
junctional
epidermolysis
bullosa
(
NH
-
JEB
)
is
a
very
rare
inherited
disorder
,
with
an
array
of
complications
.
We
present
the
case
of
a
33
-
year
-old
patient
of
Chinese
origin
,
diagnosed
with
NH
-
JEB
in
childhood
,
who
developed
severe
IgA
nephropathy
.
His
renal
impairment
was
initially
treated
by
haemodialysis
.
He
underwent
successful
renal
transplantation
,
resulting
in
normalization
of
his
renal
function
.
To
our
knowledge
,
this
is
the
first
report
of
renal
transplantation
in
a
patient
with
epidermolysis
bullosa
,
which
should
support
use
of
this
intervention
in
other
similar
cases
.
Diseases
Validation
Diseases presenting
"first report"
symptom
achondroplasia
alexander disease
aniridia
cadasil
canavan disease
child syndrome
cohen syndrome
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
cystinuria
dedifferentiated liposarcoma
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
focal myositis
harlequin ichthyosis
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
homocystinuria without methylmalonic aciduria
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kindler syndrome
krabbe disease
lamellar ichthyosis
liposarcoma
lymphangioleiomyomatosis
monosomy 21
neonatal adrenoleukodystrophy
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
pendred syndrome
pleomorphic liposarcoma
primary hyperoxaluria type 1
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
typhoid
waldenström macroglobulinemia
werner syndrome
wiskott-aldrich syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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