Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Monosomy 21, partial duplication of chromosome 11, and structural abnormality of chromosome 1q21 in a case of lymphoma developing in a transplant recipient: characteristic abnormalities of secondary lymphoma?
[monosomy 21]
Cytogenetic
analysis
by
QFQ-banding
of
direct
preparation
of
a
testicular
mass
from
a
patient
with
secondary
lymphoma
revealed
a
modal
chromosome
number
of
45
,
XY
,
including
structural
and
numerical
anomalies
.
The
most
consistent
anomalies
were
the
monosomy
21
,
duplication
of
the
long
arm
of
#
11
,
and
structural
anomaly
associated
with
chromosome
#
1
in
band
q
21
.
Diseases
Validation
Diseases presenting
"lymphoma"
symptom
adrenal incidentaloma
alpha-thalassemia
carcinoma of the gallbladder
cushing syndrome
dedifferentiated liposarcoma
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
familial hypocalciuric hypercalcemia
focal myositis
hirschsprung disease
hodgkin lymphoma, classical
kabuki syndrome
liposarcoma
locked-in syndrome
monosomy 21
oculocutaneous albinism
primary effusion lymphoma
severe combined immunodeficiency
systemic capillary leak syndrome
waldenström macroglobulinemia
wiskott-aldrich syndrome
This symptom has already been validated
