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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
"hypertension"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
aniridia
aromatase deficiency
cadasil
child syndrome
cohen syndrome
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cushing syndrome
cystinuria
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
fabry disease
familial hypocalciuric hypercalcemia
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
holt-oram syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
kallmann syndrome
kindler syndrome
lamellar ichthyosis
lymphangioleiomyomatosis
pendred syndrome
primary effusion lymphoma
scrub typhus
severe combined immunodeficiency
sneddon syndrome
typhoid
von hippel-lindau disease
well-differentiated liposarcoma
werner syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
This symptom has already been validated