MRI in Congenital Myotonic Dystrophy

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-10-6

MRI in Congenital Myotonic Dystrophy

Pediatric Neurology Briefs

Volume 6 (1992): Issue 10

By: J Gordon Millichap

Open Access

|Oct 1992

Abstract

The results of CT and MRI of the brain were analyzed and neurological development was assessed from the neonatal period in 7 children with congenital myotonic dystrophy aged 2-8 years at the Division of Neurology, Chiba Children’s Hospital and Department of Pediatrics, Chiba University School of Medicine, Chiba, Japan.

References

Tanabe Y Iai M Tamai K Fujimoto N Sugita K Neuroradiological findings in children with congenital myotonic dystrophy Acta Paediatr 1992 Aug 81 8 613 617 10.1111/j.1651-2227.1992.tb12312.x 1392386
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Cook J Gascon G Ann Neurol 1992 Sept 32 439 (abstr)
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-10-6 | Journal eISSN: 2166-6482

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Language: English

Page range: 78 - 78

Published on: Oct 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Congenital Myotonic Dystrophy,

Perinatal Asphyxia,

Cerebral Atrophy

© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 6 (1992): Issue 10