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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
.
Diseases
Validation
Diseases presenting
"telangiectasia"
symptom
coats disease
cowden syndrome
cutaneous mastocytosis
hereditary cerebral hemorrhage with amyloidosis
kallmann syndrome
kindler syndrome
malignant atrophic papulosis
omenn syndrome
pendred syndrome
severe combined immunodeficiency
systemic capillary leak syndrome
triple a syndrome
waldenström macroglobulinemia
werner syndrome
This symptom has already been validated