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Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): a case report.
[megacystis-microcolon-intestinal hypoperistalsis syndrome]
Megacystis-
microcolon
-
intestinal
hypoperistalsis
syndrome
(
MMIHS
)
is
a
rare
congenital
disorder
characterized
by
a
massively
enlarged
urinary
bladder
without
mechanical
outlet
obstruction
and
microcolon
,
as
well
as
a
hypoperistaltic
bowel
with
normal
ganglion
cell
distribution
.
We
report
one
such
case
to
discuss
the
findings
of
antenatal
ultrasound
and
the
radiologic
and
pathologic
features
of
this
condition
.