:: Volume 18, Issue 1 (1-2014) ::
IBJ 2014, 18(1): 28-33 Back to browse issues page
Molecular and Clinical Investigation of Iranian Patients with Friedreich Ataxia
Mohammad Hossein Salehi , Massoud Houshmand , Omid Aryani , Behnam Kamalidehghan , Elham Khalili
Abstract:  
Background: Friedreich ataxia (FRDA) is an autosomal recessive disorder caused by guanine-adenine-adenine (GAA) triplet expansions in the FXN gene. Its product, frataxin, which severely reduces in FRDA patients, leads to oxidative damage in mitochondria. The purpose of this study was to evaluate the triple nucleotide repeated expansions in Iranian FRDA patients and to elucidate distinguishable FRDA clinical differences in these patients. Methods: A number of 22 Iranian patients (8 females and 14 males) from 16 unrelated families were studied. DNA was extracted from the peripheral blood of patients. The frequency and length of (GAA)n repeats in intron 1 of the FXN gene were analyzed using long-range PCR. In this study, the clinical criteria of FRDA in our patients and the variability in their clinical signs were also demonstrated. Results: An inverse relationship was observed between GAA repeat size and the age of onset. Although some distinguishable clinical features (such as limb ataxia and lower limb areflexia) were found in our patients, 90-95% of them had extensor plantar response and dysarthria. The results showed only one positive diabetes patient and also different effects on eye movement abnormality among our patients. Conclusion: The onset age of symptoms showed a significant inverse correlation with allele size in our patients (P>0.05). Based on comparisons of the clinical data of all patients, clinical presentation of FRDA in Iranian patients did not differ significantly from other FRDA patients previously reported.
Keywords: Friedreich ataxia (FRDA), Frataxin, Mitochondria
Full-Text [PDF 259 kb]      
Type of Study: Full Length | Subject: Related Fields
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DOI: 10.6091/ibj.1235.2013
PMID: 24375160
PMCID: PMC3892137


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Salehi M H, Houshmand M, Aryani O, Kamalidehghan B, Khalili E. Molecular and Clinical Investigation of Iranian Patients with Friedreich Ataxia. IBJ. 2014; 18 (1) :28-33
URL: http://ibj.pasteur.ac.ir/article-1-1061-en.html
Volume 18, Issue 1 (1-2014) Back to browse issues page
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