Leigh disease-a rare mitochondrial neurometabolic disorder
PAFMJ-Pakistan Armed Forces Medical Journal. 2008; 58 (2): 229-232
in English
| IMEMR
| ID: emr-89357
ABSTRACT
Clinical presentation of Leigh's disease can be highly variable. We present here this case which presented with quite bizarre neurological symptoms and signs in early infancy and was suspected on the basis of CT scan findings which was further supported by high serum lactic acid levels
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Prognosis
/
Acidosis, Lactic
/
Magnetic Resonance Imaging
/
Tomography, X-Ray Computed
/
Mitochondrial Diseases
Type of study:
Case report
Limits:
Female
/
Humans
Language:
English
Journal:
Pak. Armed Forces Med. J.
Year:
2008
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