Literature DB >> 10771903

Spinal muscular atrophy--a clinicopathologic analysis.

V V Radhakrishnan1, M D Nair, A Kuruvilla, K Radhakrishnan, R Anandam.   

Abstract

In this retrospective study the clinical features in 16 children with spinal muscular atrophy (SMA) were reviewed and classified into three stages. The muscle biopsy specimen were routinely processed with liquid-nitrogen-isopentane and 8 micron thick frozen-sections were studied for histochemical changes. The clinical features in Type III SMA resembled with limb-girdle muscular dystrophy and the muscle biopsy was useful in distinguishing these two entities. It is being evaluated that prenatal diagnosis of SMA is possible with DNA technology developed recently in our country.

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Year:  1997        PMID: 10771903     DOI: 10.1007/bf02726126

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  6 in total

Review 1.  Chaos in classification of the spinal muscular atrophies of childhood.

Authors:  V Dubowitz
Journal:  Neuromuscul Disord       Date:  1991       Impact factor: 4.296

2.  Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3.

Authors:  L M Brzustowicz; T Lehner; L H Castilla; G K Penchaszadeh; K C Wilhelmsen; R Daniels; K E Davies; M Leppert; F Ziter; D Wood
Journal:  Nature       Date:  1990-04-05       Impact factor: 49.962

3.  Localization of the gene for X-linked spinal muscular atrophy.

Authors:  K H Fischbeck; V Ionasescu; A W Ritter; R Ionasescu; K Davies; S Ball; P Bosch; T Burns; I Hausmanowa-Petrusewicz; J Borkowska
Journal:  Neurology       Date:  1986-12       Impact factor: 9.910

4.  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

5.  Identification and characterization of a spinal muscular atrophy-determining gene.

Authors:  S Lefebvre; L Bürglen; S Reboullet; O Clermont; P Burlet; L Viollet; B Benichou; C Cruaud; P Millasseau; M Zeviani
Journal:  Cell       Date:  1995-01-13       Impact factor: 41.582

6.  Autosomal dominant spinal muscular atrophy: a clinical and genetic study.

Authors:  J Pearn
Journal:  J Neurol Sci       Date:  1978-09       Impact factor: 3.181

  6 in total

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