Literature DB >> 169177

Infantile polyneuropathy with defective myelination: an autopsy study.

S B Karch, H Urich.   

Abstract

A case is reported of a boy who developed a severe polyneuropathy in early infancy and died of respiratory failure at the age of 18 months. Autopsy revealed almost total lack of myelin sheaths in the cranial, spinal and peripheral nerves. The defect involved the entire peripheral nervous system and was confined to it, central myelination being normal. It is suggested that this case is another example of the condition described by Lyon (1969) and by Kennedy et al. (1971) in which pathological observations were confined to biopsy material. In spite of some similarities between these cases and those of hypertrophic neuropathy reported by Déjerine and Sottas in 1893, they seem to form a distinct sub-group, possibly even a separate entity: infantile polyneuropathy with defective myelination.

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Year:  1975        PMID: 169177     DOI: 10.1111/j.1469-8749.1975.tb03502.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  11 in total

1.  Variability of morphological features in early infantile polyneuropathy with defective myelination.

Authors:  A Vital; C Vital; J P Riviere; C Brechenmacher; J Marot
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

2.  Congenital hypo- and hypermyelination neuropathy. Two cases.

Authors:  J M Vallat; R Gil; M J Leboutet; J Hugon; D Moulies
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

3.  A case report of congenital hypomyelination.

Authors:  J Ono; E Senba; S Okada; J Abe; Y Futagi; H Shimizu; T Sugita; S Hashimoto; H Yabuuchi
Journal:  Eur J Pediatr       Date:  1982-05       Impact factor: 3.183

4.  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

5.  Congenital neuropathy with prevailing axonal changes. A clinical and histological report.

Authors:  F Guzzetta; G Ferrière
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

6.  Connatal polyneuropathy -- a case with proliferated microfilaments in Schwann cells.

Authors:  J Ulrich; H R Hirt; P Kleihues; M Oberholzer
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

7.  Congenital hypomyelinating neuropathy.

Authors:  Y Harati; I J Butler
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-12       Impact factor: 10.154

Review 8.  Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.

Authors:  Anneke Gabreëls-Festen
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

9.  Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.

Authors:  Oranee Sanmaneechai; Shawna Feely; Steven S Scherer; David N Herrmann; Joshua Burns; Francesco Muntoni; Jun Li; Carly E Siskind; John W Day; Matilde Laura; Charlotte J Sumner; Thomas E Lloyd; Sindhu Ramchandren; Rosemary R Shy; Tiffany Grider; Chelsea Bacon; Richard S Finkel; Sabrina W Yum; Isabella Moroni; Giuseppe Piscosquito; Davide Pareyson; Mary M Reilly; Michael E Shy
Journal:  Brain       Date:  2015-08-25       Impact factor: 13.501

10.  Autosomal recessive hypermyelinating neuropathy.

Authors:  M Sabatelli; T Mignogna; G Lippi; S Servidei; G Manfredi; E Ricci; E Bertini; M Lo Monaco; P Tonali
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

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