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Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia.
[aniridia]
We
report
on
a
boy
presenting
submucous
cleft
palate
,
hydronephrosis
,
ventriculoseptal
defect
,
aniridia
,
and
developmental
delay
.
Additional
material
on
11
p
13
was
cytogenetically
visible
and
array
analyses
identified
a
duplicated
segment
on
15
q
25
-
26
chromosome
region
;
further
,
array
analyses
revealed
a
small
deletion
(
49
kb
)
at
11
p
13
region
involving
the
ELP
4
gene
and
a
duplication
at
8
p
23
.
1
.
Results
were
confirmed
with
both
molecular
and
molecular
cytogenetics
techniques
.
Possibilities
for
etiological
basis
of
clinical
phenotype
are
discussed
.
Diseases
Validation
Diseases presenting
"hydronephrosis"
symptom
aniridia
cystinuria
erdheim-chester disease
hirschsprung disease
hydrocephalus with stenosis of the aqueduct of sylvius
kindler syndrome
megacystis-microcolon-intestinal hypoperistalsis syndrome
This symptom has already been validated