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Research Article

Spinal Muscular Atrophy Due to Double Gene Conversion Event

, , , , , , & show all
Pages 107-111 | Received 02 Jul 2010, Published online: 03 Nov 2010
 

ABSTRACT

Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by degeneration of the anterior horn cells of the spinal cord. The survival motor neuron (SMN) gene has been identified as an SMA-determining gene. SMN exists as two copies in 5q13, and deletions in exons 7 and 8 of the telomeric copy (SMNT) occur in 95% of patients, regardless of disease severity. In a minority of patients, exon 7 but not exon 8 of SMNT appears deleted. We now report a patient with typical features of SMA type II who carried homozygous deletions of SMNT exon 7 and centromeric SMN (SMNC) exon 8 but retained SMNT exon 8 and SMNC exon 7. Sequence analysis demonstrated that SMNC exon 7 was adjacent to SMNT exon 8 on both SMN copies, indicating a double conversion. We confirm that sequence conversion is a common event in SMA and is associated with the milder form of the disease. The severity, however, can be modified in either positive or negative direction by other factors.

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