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Hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia [corrected].
[kallmann syndrome]
A
65
-
year
-old
man
was
referred
to
our
clinic
for
the
rehabilitation
of
right
hemiparesis
caused
by
ischaemic
stroke
.
Hypertension
,
postphlebitic
syndrome
of
lower
limbs
,
frequent
nose
bleeding
,
and
anemia
were
present
in
his
history
;
in
his
adolescence
,
he
was
treated
for
idiopathic
hypogonadotropic
hypogonadism
.
Further
investigations
have
revealed
also
microsomia
,
suggesting
a
clinical
diagnosis
of
Kallmann
syndrome
,
that
is
,
an
association
,
possible
in
males
and
females
,
of
hypogonadotropic
hypogonadism
with
olfactory
deficits
.
A
definite
diagnosis
of
hereditary
hemorrhagic
telangiectasia
was
made
based
on
clinical
criteria
and
confirmed
by
genetic
analysis
.