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Acta Gastroenterol Belg ; 72(3): 365-8, 2009.
Article in English | MEDLINE | ID: mdl-19902874

ABSTRACT

We describe a patient in whom abdominal pain and vomiting were the presenting symptoms of Mitochondrial Myopathy Encephalopathy, Lactic Acidosis with Stroke-like episodes syndrome (MELAS). Mitochondrial disorders usually present with neurological symptoms or with myopathic features at any age. Although many patients develop visceral symptoms at a certain moment during the course of the disease, only in a minority of patients these symptoms are the unique presenting ones. The proband was initially diagnosed as having gastro-oesophageal reflux and it was only after detailed clinical history that an underlying metabolic defect was suspected and the molecular defect identified.


Subject(s)
Abdominal Pain/complications , MELAS Syndrome/diagnosis , Vomiting/complications , Child , Humans , MELAS Syndrome/complications , Male
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