Rare Diseases Symptoms Automatic Extraction
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A random Abstract
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Two novel missense mutations in the aspartoacylase gene in a Chinese patient with congenital Canavan disease.
[canavan disease]
We
herein
describe
the
first
Chinese
case
of
Canavan
disease
diagnosed
by
biochemical
analysis
and
confirmed
by
DNA
studies
.
We
report
two
novel
mutations
:
c
.
2
T
>
C
/
M
1
T
,
an
initiation
codon
mutation
,
and
c
.
209
A
>
G
/
N
70
S
,
which
is
located
at
the
enzyme-substrate
binding
site
.
The
combination
of
these
two
mutations
resulted
in
a
congenital
form
of
Canavan
disease
.
Diseases
Validation
Diseases presenting
"congenital form"
symptom
canavan disease
hydrocephalus with stenosis of the aqueduct of sylvius
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