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Unusual pedigree patterns in seven families with spinal muscular atrophy; further evidence for the allelic model hypothesis.

作者信息

Bouwsma G, Leschot N J

出版信息

Clin Genet. 1986 Sep;30(3):145-9. doi: 10.1111/j.1399-0004.1986.tb00586.x.

DOI:10.1111/j.1399-0004.1986.tb00586.x
PMID:3780029
Abstract

Clinical and genetic findings are presented in 18 patients, from 7 pedigrees with different types of spinal muscular atrophy (SMA). The SMA diagnosis was based on EMG and muscle biopsy findings. All 7 pedigrees show an unusual genetic pattern, not consistent with simple autosomal recessive inheritance. Furthermore, in 6 of the 7 pedigrees different types of SMA were present within each pedigree. Our findings can be explained by an extension of a multiple alleles hypothesis originally described by Becker in 1964.

摘要

相似文献

1
Unusual pedigree patterns in seven families with spinal muscular atrophy; further evidence for the allelic model hypothesis.
Clin Genet. 1986 Sep;30(3):145-9. doi: 10.1111/j.1399-0004.1986.tb00586.x.
2
Becker's allelic model to explain unusual pedigrees with spinal muscular atrophy.
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引用本文的文献

1
Perspectives in genetic counseling for spinal muscular atrophy in the new therapeutic era: early pre-symptomatic intervention and test in minors.新治疗时代脊髓性肌萎缩症遗传咨询的观点:未成年人的早期症状前干预和检测。
Eur J Hum Genet. 2019 Dec;27(12):1774-1782. doi: 10.1038/s41431-019-0415-4. Epub 2019 May 3.
2
SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings.生存运动神经元2(SMN2)基因拷贝数可预测急性或慢性脊髓性肌萎缩症,但无法解释同胞间的家族内变异性。
J Neurol. 2006 Jan;253(1):21-5. doi: 10.1007/s00415-005-0912-y. Epub 2005 Jun 28.
3
Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw.
Hum Genet. 1990 Jul;85(2):211-4. doi: 10.1007/BF00193198.
4
Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.婴儿脊髓性肌萎缩症(SMA)与同胞中的多发性先天性骨折:一种致死性新综合征。
J Med Genet. 1991 May;28(5):345-8. doi: 10.1136/jmg.28.5.345.
5
Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5q.同一同胞关系中的脊髓性肌萎缩症(SMA)II型和III型近端型并非由5号染色体上SMA位点的不同等位基因引起。
Am J Hum Genet. 1992 May;50(5):892-5.
6
Prenatal prediction of spinal muscular atrophy.
J Med Genet. 1992 Mar;29(3):165-70. doi: 10.1136/jmg.29.3.165.