Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Isolation of Toxoplasma gondii strains similar to Africa 1 genotype in Turkey.
[congenital toxoplasmosis]
Toxoplasma
gondii
is
a
protozoon
parasite
that
has
a
worldwide
dissemination
.
It
can
cause
serious
clinical
problems
such
as
congenital
toxoplasmosis
,
retinochoroiditis
,
and
encephalitis
.
Currently
,
T
.
gondii
genotypes
are
being
associated
with
these
clinical
presentations
which
may
help
clinicians
design
their
treatment
strategy
.
Two
T
.
gondii
strains
named
Ankara
and
Ege-
1
were
isolated
from
newborns
with
congenital
toxoplasmosis
in
Central
and
Western
Anatolia
,
respectively
.
Ankara
and
Ege-
1
strains
were
isolated
from
the
cerebrospinal
fluid
of
newborns
.
According
to
microsatellite
analysis
,
Ankara
and
Ege-
1
strains
were
sorted
as
Africa
1
genotype
.
T
.
gondii
strains
isolated
in
Turkey
were
first
time
genotyped
in
this
study
.
Africa
1
genotype
has
previously
been
isolated
in
immunosuppressed
patients
originating
from
sub-
Saharan
Africa
.
The
reason
of
detecting
a
strain
mainly
detected
in
Africa
can
be
associated
with
Turkey
's
specific
geographical
location
.
Turkey
is
like
a
bridge
between
Asia
,
Europe
and
Africa
.
Historically
,
Anatolia
was
on
the
Silk
Road
and
other
trading
routes
that
ended
in
Europe
.
Thus
,
detecting
Africa
1
strain
in
Anatolia
can
be
anticipated
.
Consequently
,
strains
detected
mainly
in
Europe
and
Asia
may
also
be
detected
in
Anatolia
and
vice
versa
.
Therefore
,
further
studies
are
required
to
isolate
more
strains
from
Turkey
.
Diseases
Validation
Diseases presenting
"first time"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
congenital adrenal hyperplasia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
gm1 gangliosidosis
harlequin ichthyosis
heparin-induced thrombocytopenia
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom