Literature DB >> 8374922

Neonatal peripheral hypotonia: clinical and electromyographic characteristics.

E Parano1, R E Lovelace.   

Abstract

Hypotonia is a common occurrence in pediatrics, especially in the neonatal period. The hypotonic neonate represents a diagnostic challenge for the general pediatrician because hypotonia may be caused by a lesion at any level in the neuraxis: (1) central nervous system (CNS), (2) peripheral nerves (PN), (3) neuromuscular junction, or (4) muscles. Distinguishing among these pathologies is a particularly arduous task. This review will discuss the clinical approach to neonatal hypotonia with emphasis on disorders of the peripheral nervous system and muscle, and the importance of the electrophysiological study as a diagnostic test.

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Year:  1993        PMID: 8374922     DOI: 10.1007/bf00272270

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  20 in total

Review 1.  Mitochondrial defects of brain and muscle.

Authors:  D C De Vivo; S DiMauro
Journal:  Biol Neonate       Date:  1990

Review 2.  Myopathies of infancy and childhood.

Authors:  G Miller
Journal:  Pediatr Ann       Date:  1989-07       Impact factor: 1.132

Review 3.  Central nervous system disorders producing hypotonia.

Authors:  W W Wasiewski
Journal:  Pediatr Ann       Date:  1989-07       Impact factor: 1.132

4.  Diagnosis and management of diseases affecting the motor unit in infancy.

Authors:  H C Maguire; J T Sladky
Journal:  R I Med J       Date:  1989-10

5.  The pathophysiology of the floppy infant.

Authors:  E L Zalneraitis
Journal:  R I Med J       Date:  1989-10

6.  Evaluation of the floppy infant, or congenital hypotonia.

Authors:  A S Fremion
Journal:  Indiana Med       Date:  1986-08

7.  Benign congenital hypotonia. A clinical study in 43 children.

Authors:  A Shuper; R Weitz; I Varsano; M Mimouni
Journal:  Eur J Pediatr       Date:  1987-07       Impact factor: 3.183

8.  The diagnostic value of electromyography in infantile hypotonia.

Authors:  R J Packer; M J Brown; P H Berman
Journal:  Am J Dis Child       Date:  1982-12

9.  Newborn infants to myasthenic mothers: a clinical study and an investigation of acetylcholine receptor antibodies in 17 children.

Authors:  A K Lefvert; P O Osterman
Journal:  Neurology       Date:  1983-02       Impact factor: 9.910

10.  The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.

Authors:  R A Ouvrier; J G McLeod; T E Conchin
Journal:  Brain       Date:  1987-02       Impact factor: 13.501

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