Transient cytoplasmic bodies in muscle of three infants with werdnig-hoffmann disease

John J. Buchino, Kevin E. Bove, Susan T. Iannaccone

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

We present three instances in which cytoplasmic bodies in muscle fibers were associated with Werdnig-Hoffmann disease. The children presented within the first 6 weeks of life with clinical symptoms and laboratory studies indicative of infantile spinomuscular atrophy (ISMA). Initial muscle biopsies in each case revealed signs of muscle immaturity and cytoplasmic bodies but lacked features of denervation. Follow-up biopsies in 2 cases revealed changes typical of ISMA, but cytoplasmic bodies were no longer present. A follow-up biopsy was not available in the third child who also had a clinical course consistent with ISMA. We discuss the pathogenesis of cytoplasmic bodies and their significance in association with Werdnig-Hoffmann disease..

Original languageEnglish (US)
Pages (from-to)563-573
Number of pages11
JournalFetal and Pediatric Pathology
Volume10
Issue number4
DOIs
StatePublished - 1990

Fingerprint

Spinal Muscular Atrophies of Childhood
Atrophy
Biopsy
Muscles
Denervation

Keywords

  • Cytoplasmic bodies
  • Infantile spinomuscular atrophy
  • Werdnig-Hoffmann disease

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Pediatrics, Perinatology, and Child Health

Cite this

Transient cytoplasmic bodies in muscle of three infants with werdnig-hoffmann disease. / Buchino, John J.; Bove, Kevin E.; Iannaccone, Susan T.

In: Fetal and Pediatric Pathology, Vol. 10, No. 4, 1990, p. 563-573.

Research output: Contribution to journalArticle

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