Literature DB >> 745212

Genetic studies of acute infantile spinal muscular atrophy (SMA type I). An analysis of sex ratios, segregation ratios, and sex influence.

J Pearn.   

Abstract

An analysis of segregation and sex ratios, and of sex influence, was undertaken in a series of 78 index patients with acute infantile spinal muscular atrophy (SMA type I). The sex ratio of index patients was 2.0, and the excess of males was shown to occur principally among sporadic cases. The sex ratio of familial cases did not differ significantly from 1.0. The implications of this are discussed. No sex influence on age at onset, or on life expectancy, was present. The segregation ratio (Weinberg Proband method) was 0.29 for all index cases, and 0.26 for all cases excluding those referred specifically to a genetic counselling clinic. Autosomal recessivity is confirmed for this disease, with the probable inclusion of unrecognised male phenocopies in clinical series.

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Year:  1978        PMID: 745212      PMCID: PMC1013754          DOI: 10.1136/jmg.15.6.414

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  10 in total

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2.  The genetic component in child mortality.

Authors:  D F Roberts; J Chavez; S D Court
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3.  The genetic identity of acute infantile spinal muscular atrophy.

Authors:  J H Pearn; C O Carter; J Wilson
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4.  Fetal movements and Werdnig-Hoffmann disease.

Authors:  J H Pearn
Journal:  J Neurol Sci       Date:  1973-04       Impact factor: 3.181

5.  The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England.

Authors:  J H Pearn
Journal:  J Med Genet       Date:  1973-09       Impact factor: 6.318

6.  Genetics of childhood spinal muscular atrophy.

Authors:  E J Winsor; E G Murphy; M W Thompson; T E Reed
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Review 7.  The nosology of the spinal muscular atrophies.

Authors:  A E Emery
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

8.  International collaborative study of the spinal muscular atrophies. Part 2. Analysis of genetic data.

Authors:  A E Emery; A M Davie; S Holloway; R skinner
Journal:  J Neurol Sci       Date:  1976-12       Impact factor: 3.181

9.  Acute Werdnig-Hoffmann disease: acute infantile spinal muscular atrophy.

Authors:  J H Pearn; J Wilson
Journal:  Arch Dis Child       Date:  1973-06       Impact factor: 3.791

10.  A clinical and genetic study of chronic proximal spinal muscular atrophy.

Authors:  S Bundey; R E Lovelace
Journal:  Brain       Date:  1975-09       Impact factor: 13.501

  10 in total
  8 in total

1.  Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw.

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2.  A clinical, epidemiological and genetic study of hereditary motor neuropathies in Benghazi, Libya.

Authors:  K Radhakrishnan; A K Thacker; J C Maloo
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Journal:  Hum Genet       Date:  2008-12-03       Impact factor: 4.132

5.  Clinical study of proximal spinal muscular atrophy. Report on 89 cases.

Authors:  P Tonali; S Servidei; A Uncini; D Restuccia; G Galluzzi
Journal:  Ital J Neurol Sci       Date:  1984-12

6.  Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.

Authors:  Z Borochowitz; B Glick; S Blazer
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318

7.  Identification of a novel cyclic AMP-response element (CRE-II) and the role of CREB-1 in the cAMP-induced expression of the survival motor neuron (SMN) gene.

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8.  Abnormal mitochondrial transport and morphology as early pathological changes in human models of spinal muscular atrophy.

Authors:  Chong-Chong Xu; Kyle R Denton; Zhi-Bo Wang; Xiaoqing Zhang; Xue-Jun Li
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  8 in total

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