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Paper Information

Journal:   IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)   FEBRUARY 2008 , Volume 2 , Number 2; Page(s) 47 To 50.
 
Paper: 

MLASA SYNDROME: A CASE REPORT

 
 
Author(s):  FALAH R.*
 
* SHAHEED SADOUGHI UNIVERSITY OF MEDICAL SCIENCES
 
Abstract: 
Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) syndrome is a rare autosomal recessive disorder of oxidative phosphorylation and iron metabolism. The association between myopathy and sideroblastic anemia was initially reported in 1974. Here we report an 8.5 year old boy with normal cognitive function, suffering from chronic progressive weakness in his lower extremities, inability to walk and palor. Microcytic sideroblastic anemia, mild lactic acidosis and inflammatory myopathy (myositis) in muscle biopsy was detected and treated; the response to corticosteroid therapy and rehabilitation was excellent and the patient was ambulatory after four months.
 
Keyword(s): SIDEROBLASTIC ANEMIA, MITOCHONDRIAL MYOPATHY, LACTIC ACIDOSIS
 
 
References: 
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Citations: 
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+ Click to Cite.
APA: Copy

FALAH, R. (2008). MLASA SYNDROME: A CASE REPORT. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 2(2), 47-50. https://www.sid.ir/en/journal/ViewPaper.aspx?id=106854



Vancouver: Copy

FALAH R.. MLASA SYNDROME: A CASE REPORT. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN). 2008 [cited 2021June18];2(2):47-50. Available from: https://www.sid.ir/en/journal/ViewPaper.aspx?id=106854



IEEE: Copy

FALAH, R., 2008. MLASA SYNDROME: A CASE REPORT. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), [online] 2(2), pp.47-50. Available: https://www.sid.ir/en/journal/ViewPaper.aspx?id=106854.



 
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