Myoneurogenic gastrointestinal encephalopathy

Myoneurogenic gastrointestinal encephalopathy

Infobox_Disease
Name = PAGENAME


Caption =
DiseasesDB = 32948
ICD10 =
ICD9 = ICD9|277.87
ICDO =
OMIM = 603041
MedlinePlus =
eMedicineSubj =
eMedicineTopic =
MeshID =

Myoneurogenic gastrointestinal encephalopathy or MNGIE is a rare mitochondrial disease typically appearing between the second and fifth decades of life.

Presentation

MNGIE is a multisystem disorder causing ptosis, progressive external ophthalmoplegia, gastrointestinal dysmotility (often pseudoobstruction), diffuse leukoencephalopathy, thin body habitus, peripheral neuropathy, and myopathy.


Wikimedia Foundation. 2010.

Игры ⚽ Нужно сделать НИР?

Look at other dictionaries:

  • Mitochondrial disease — Classification and external resources Micrograph showing ragged red fibres, a finding seen in mitochondrial diseases. Muscle biopsy. Gomori trichrome stain …   Wikipedia

Share the article and excerpts

Direct link
… Do a right-click on the link above
and select “Copy Link”