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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
"corpus callosum"
symptom
adrenomyeloneuropathy
alexander disease
cadasil
canavan disease
classical phenylketonuria
cohen syndrome
gm1 gangliosidosis
hirschsprung disease
hydrocephalus with stenosis of the aqueduct of sylvius
kabuki syndrome
kallmann syndrome
krabbe disease
monosomy 21
neonatal adrenoleukodystrophy
oligodontia
proteus syndrome
pyruvate dehydrogenase deficiency
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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