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Panhypopituitary insufficiency in a patient with clinical diagnosis of Chitayat-Hall syndrome.
[wolf-hirschhorn syndrome]
We
report
an
8
-
year
-old
proband
with
severe
motor
and
intellectual
disability
presenting
a
variety
of
dysmorphic
features
such
as
microcephaly
,
prominent
glabella
(
ridged
metopic
suture
)
and
congenital
distal
limb
contractures
.
As
well
as
panhypopituitary
insufficiency
,
brain
defects
,
e
.
g
.
agenesis
of
corpus
callosum
,
colpocephaly
,
and
pachygyria
as
well
as
strabismus
and
tracheo-
laryngeal
hypoplasia
,
were
diagnosed
.
Genetic
examination
revealed
a
normal
karyotype
and
excluded
Wolf-
Hirschhorn
syndrome
and
subtelomeric
deletions
.
Chitayat-
Hall
syndrome
was
diagnosed
based
on
clinical
traits
.
Diseases
Validation
Diseases presenting
"strabismus"
symptom
aniridia
classical phenylketonuria
coats disease
cohen syndrome
congenital toxoplasmosis
focal myositis
holt-oram syndrome
homocystinuria without methylmalonic aciduria
kabuki syndrome
oculocutaneous albinism
oligodontia
proteus syndrome
well-differentiated liposarcoma
wolf-hirschhorn syndrome
This symptom has already been validated