Literature DB >> 3977387

Diaphragmatic paralysis due to spinal muscular atrophy. An unrecognised cause of respiratory failure in infancy?

R C McWilliam, D Gardner-Medwin, D Doyle, J B Stephenson.   

Abstract

An unusual form of spinal muscular atrophy presenting with respiratory failure was observed in four infants from two families. In one, whose death was attributed to pneumonia, the diagnosis was inferred retrospectively after two siblings died from an identical illness and were shown to have diaphragmatic paralysis and the typical electrophysiological and histological features of spinal muscular atrophy. Other signs of skeletal muscular weakness were absent or inconspicuous. The fourth, unrelated infant presented in an identical way but has survived for over a year on a ventilator. Two months after the onset of respiratory paralysis, more extensive skeletal muscular weakness was seen. Other infants, dying of unexplained respiratory illness, may have this disorder and some may be included in the miscellany of disorders that constitute the sudden infant death syndrome.

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Mesh:

Year:  1985        PMID: 3977387      PMCID: PMC1777133          DOI: 10.1136/adc.60.2.145

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  13 in total

1.  Infantile muscular atrophy.

Authors:  R K BYERS; B Q BANKER
Journal:  Arch Neurol       Date:  1961-08

2.  Chest wall mechanics and respiratory muscles in infants.

Authors:  N L Muller; A C Bryan
Journal:  Pediatr Clin North Am       Date:  1979-08       Impact factor: 3.278

3.  Transient bilateral diaphragmatic paralysis.

Authors:  S A Spitzer; A D Korczyn; J Kalaci
Journal:  Chest       Date:  1973-09       Impact factor: 9.410

4.  Electromyography and muscle biopsy in infantile spinal muscular atrophy.

Authors:  F Buchthal; P Z Olsen
Journal:  Brain       Date:  1970       Impact factor: 13.501

5.  A neuropathologic study of Werdnig-Hoffmann disease with special reference to the thalamus and posterior roots.

Authors:  K Shishikura; M Hara; Y Sasaki; K Misugi
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

6.  Bilateral diaphragmatic paralysis in the newborn infant.

Authors:  T K Aldrich; J H Herman; D F Rochester
Journal:  J Pediatr       Date:  1980-12       Impact factor: 4.406

7.  The sudden infant death syndrome: repetitions in families.

Authors:  D R Peterson; N M Chinn; L D Fisher
Journal:  J Pediatr       Date:  1980-08       Impact factor: 4.406

8.  Motor nerve conduction velocity in spinal muscular atrophy of childhood.

Authors:  A Moosa; V Dubowitz
Journal:  Arch Dis Child       Date:  1976-12       Impact factor: 3.791

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 study of chronic childhood spinal muscular atrophy. A review of 141 cases.

Authors:  J H Pearn; D Gardner-Medwin; J Wilson
Journal:  J Neurol Sci       Date:  1978-08       Impact factor: 3.181

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  5 in total

Review 1.  Diaphragmatic paresis: pathophysiology, clinical features, and investigation.

Authors:  G J Gibson
Journal:  Thorax       Date:  1989-11       Impact factor: 9.139

2.  Vocal cord paralysis as a presenting sign of acute spinal muscular atrophy SMA type 1.

Authors:  E Roulet; T Deonna
Journal:  Arch Dis Child       Date:  1992-03       Impact factor: 3.791

3.  Spinal muscular atrophy genetic testing experience at an academic medical center.

Authors:  Shuji Ogino; Debra G B Leonard; Hanna Rennert; Robert B Wilson
Journal:  J Mol Diagn       Date:  2002-02       Impact factor: 5.568

4.  Diaphragmatic paralysis due to spinal muscular atrophy.

Authors:  N P Murphy; D C Davidson; J Bouton
Journal:  Arch Dis Child       Date:  1985-05       Impact factor: 3.791

5.  Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13.

Authors:  G Novelli; F Capon; L Tamisari; E Grandi; C Angelini; P Guerrini; B Dallapiccola
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

  5 in total

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