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Wolf-Hirschhorn syndrome: a case study and disease overview.
[wolf-hirschhorn syndrome]
Wolf-
Hirschhorn
syndrome
is
caused
by
a
deletion
of
a
segment
on
the
short
arm
(
p
)
of
chromosome
4
.
The
major
features
of
this
disorder
include
a
characteristic
facial
appearance
known
as
the
"
Greek
helmet
,
"
delayed
growth
and
development
;
prenatally
and
postnatally
,
intellectual
disabilities
,
and
seizures
.
To
provide
comprehensive
and
appropriate
nursing
and
medical
care
to
infants
with
Wolf-
Hirschhorn
syndrome
,
it
is
imperative
to
know
and
understand
the
disorder
.
A
case
study
of
a
36
weeks
'
gestational
age
white
-
Hispanic
male
infant
with
Wolf-
Hirschhorn
syndrome
is
presented
with
the
purpose
of
increasing
clinical
knowledge
and
the
implications
for
the
clinical
nurse
and
neonatal
nurse
practitioner
.
