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A clonal dic(16;21)(p13.1;p11.2)del(16)(q11.1), with gains of several chromosomes and monosomy 21, in a case of splenic hamartoma: evidence for its neoplastic, not hamartomatous, origin.
[monosomy 21]
Cytogenetic
examination
of
a
case
of
splenic
hamartoma
led
to
the
discovery
of
a
clonal
population
with
the
karyotype
47
approximately
58
,
XX
,
+
X
,
+
4
,
+
5
,
+
5
,
+
6
,
+
10
,
+
12
,
+
14
,
der
(
16
)
dic
(
16
;
21
)
(
p
13
.
3
;
p
11
.
2
)
,
dic
(
16
;
21
)
del
(
16
)
(
q
11
.
1
)
,
+
17
,
+
19
,
+
20
,
-
21
.
This
finding
is
indicative
of
a
neoplastic
,
not
hamartomatous
,
origin
for
this
lesion
.
Diseases
Validation
Diseases presenting
"hamartoma"
symptom
coats disease
cowden syndrome
focal myositis
liposarcoma
monosomy 21
pendred syndrome
proteus syndrome
werner syndrome
This symptom has already been validated