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Megacystis-microcolon-intestinal hypoperistalsis syndrome: report of one case.
[megacystis-microcolon-intestinal hypoperistalsis syndrome]
Megacystis-
microcolon
-
intestinal
hypoperistalsis
syndrome
(
MMIHS
)
is
a
very
rare
congenital
disease
characterized
by
abdominal
distension
due
to
a
dilated
urinary
bladder
,
microcolon
and
decreased
or
absent
intestinal
peristalsis
.
Most
patients
die
at
an
early
age
.
We
report
on
a
female
baby
with
this
syndrome
which
was
associated
with
duodenal
web
and
tracheobronchial
malacia
.
The
literature
on
this
syndrome
is
also
reviewed
.