<it>SMN1 </it>dosage analysis in spinal muscular atrophy from India

<p>Abstract</p> <p>Background</p> <p>Spinal muscular atrophy (SMA) represents the second most common fatal autosomal recessive disorder after cystic fibrosis. Due to the high carrier frequency, the burden of this genetic disorder is very heavy in developing countries li...

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Main Authors: Leonard Debra GB (Author), Rennert Hanna (Author), Kesari Akanchha (Author), Mittal Balraj (Author)
Format: Book
Published: BMC, 2005-05-01T00:00:00Z.
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001 doaj_e5f3fa085f624e5eb46a551e7f1ecec2
042 |a dc 
100 1 0 |a Leonard Debra GB  |e author 
700 1 0 |a Rennert Hanna  |e author 
700 1 0 |a Kesari Akanchha  |e author 
700 1 0 |a Mittal Balraj  |e author 
245 0 0 |a <it>SMN1 </it>dosage analysis in spinal muscular atrophy from India 
260 |b BMC,   |c 2005-05-01T00:00:00Z. 
500 |a 10.1186/1471-2350-6-22 
500 |a 1471-2350 
520 |a <p>Abstract</p> <p>Background</p> <p>Spinal muscular atrophy (SMA) represents the second most common fatal autosomal recessive disorder after cystic fibrosis. Due to the high carrier frequency, the burden of this genetic disorder is very heavy in developing countries like India. As there is no cure or effective treatment, genetic counseling becomes very important in disease management. <it>SMN1 </it>dosage analysis results can be utilized for identifying carriers before offering prenatal diagnosis in the context of genetic counseling.</p> <p>Methods</p> <p>In the present study we analyzed the carrier status of parents and sibs of proven SMA patients. In addition, <it>SMN1 </it>copy number was determined in suspected SMA patients and parents of children with a clinical diagnosis of SMA.</p> <p>Results</p> <p>wenty nine DNA samples were analyzed by quantitative PCR to determine the number of <it>SMN1 </it>gene copies present, and 17 of these were found to have one <it>SMN1 </it>gene copy. The parents of confirmed SMA patients were found to be obligate carriers of the disease. Dosage analysis was useful in ruling out clinical suspicion of SMA in four patients. In a family with history of a deceased floppy infant and two abortions, both parents were found to be carriers of SMA and prenatal diagnosis could be offered in future pregnancies.</p> <p>Conclusion</p> <p><it>SMN1 </it>copy number analysis is an important parameter for identification of couples at risk for having a child affected with SMA and reduces unwarranted prenatal diagnosis for SMA. The dosage analysis is also useful for the counseling of clinically suspected SMA with a negative diagnostic SMA test.</p> 
546 |a EN 
690 |a Internal medicine 
690 |a RC31-1245 
690 |a Genetics 
690 |a QH426-470 
655 7 |a article  |2 local 
786 0 |n BMC Medical Genetics, Vol 6, Iss 1, p 22 (2005) 
787 0 |n http://www.biomedcentral.com/1471-2350/6/22 
787 0 |n https://doaj.org/toc/1471-2350 
856 4 1 |u https://doaj.org/article/e5f3fa085f624e5eb46a551e7f1ecec2  |z Connect to this object online.