Literature DB >> 6288385

A case report of congenital hypomyelination.

J Ono, E Senba, S Okada, J Abe, Y Futagi, H Shimizu, T Sugita, S Hashimoto, H Yabuuchi.   

Abstract

A 3 year, 11 month-old Japanese male with congenital hypomyelination is described. Clinical features are delay of motor development, generalized muscle hypotonia and weakness, absent tendon reflexes due to peripheral neuropathy, and normal mental development. Electrophysiologically, nerve conduction velocities could not be measured. Histological examination of the right sural nerve revealed total of absence myelin of most of the myelinated fibers. Electronmicroscopically, there was a concentric network of lamellae formed by double-layered sheets of basement membranes with fragments of Schwann cell cytoplasm around the myelinated fibers, so called "onion-bulbs". These peculiar features were similar to those in the cases reported by Lyon, (1969); Kennedy et al., (1977); Karch et al., (1975); and Anderson et al. (1973).

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Year:  1982        PMID: 6288385     DOI: 10.1007/bf00441215

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  7 in total

1.  Infantile polyneuropathy with defective myelination: an autopsy study.

Authors:  S B Karch; H Urich
Journal:  Dev Med Child Neurol       Date:  1975-08       Impact factor: 5.449

2.  A case of congenital hypomyelination neuropathy. Clinical, morphological, and chemical studies.

Authors:  W R Kennedy; J H Sung; J F Berry
Journal:  Arch Neurol       Date:  1977-06

3.  Hypertrophic neuropathy with primary failure of peripheral myelination.

Authors:  W R Kennedy; J H Sung; J F Berry; A Mastri
Journal:  Trans Am Neurol Assoc       Date:  1971

4.  Hypertrophic interstitial polyneuropathy in infancy. Clinical and pathologic features in two cases.

Authors:  R M Anderson; X Dennett; I J Hopkins; L K Shield
Journal:  J Pediatr       Date:  1973-04       Impact factor: 4.406

5.  Ultrastructural study of a nerve biopsy from a case of early infantile chronic neuropathy.

Authors:  G Lyon
Journal:  Acta Neuropathol       Date:  1969       Impact factor: 17.088

6.  Electron-microscopic heterogeneity of onion-bulb neuropathies of the Déjerine-Sottas type. Two patients in one family with the variant described by Lyon (1969).

Authors:  E Joosten; F Gabreëls; A Gabrèèls-Festen; G Vrensen; J Korten; S Notermans
Journal:  Acta Neuropathol       Date:  1974-02-28       Impact factor: 17.088

7.  Chronic neuropathy presenting as a floppy infant with respiratory distress.

Authors:  R B Moss; S Sriram; K A Kelts; L S Forno; N J Lewiston
Journal:  Pediatrics       Date:  1979-10       Impact factor: 7.124

  7 in total
  5 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 hypomyelination with axonopathy.

Authors:  A Vital; C Vital; M Coquet; X Hernandorena; J M Demarquez
Journal:  Eur J Pediatr       Date:  1989-02       Impact factor: 3.183

3.  MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.

Authors:  N Tachi; N Kozuka; K Ohya; S Chiba; M Naganuma
Journal:  Neuroradiology       Date:  1995-08       Impact factor: 2.804

4.  Congenital hypomyelinating neuropathy.

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

Review 5.  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

  5 in total

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