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Congenital Myotonic Dystrophy Cover
Open Access
|Sep 1987

Full Article

Ten infants with congenital myotonic dystrophy admitted to the Dept Pediatrics and Neonatal Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, London, 1982-86, were investigated by ultrasonography or CT brain scans between 1 day and 2 months of age. The infants presented with generalized hypotonia, facial diplegia, and respiratory and feeding difficulties, and the diagnosis was confirmed by demonstrating maternal myotonia.

Cerebral ventricular dilation was demonstrated in 8 (80%) infants, and 3 were scanned on the first day of life. Neonatal asphyia occurred in 7, associated with intraventricular hemorrhage (IVH) in 2. One had subarachnoid hemorrhage and one showed infarcts in the white matter. The pathogenesis of ventricular dilation in congenital myotonic dystrophy was probably IVH in 2, but a developmental anomaly during fetal life was the more likely explanation in the remainder. The authors note that mental retardation in 70% of cases can be related to the ventricular dilation which may be progressive and require surgical treatment. [1]

COMMENT: It may be impolite to shake hands with a lady! But a handshake for a mother of a floppy baby with respiratory distress may be diagnostic of myotonia and is good clinical practice. Dr. Koh of Hope Hosp, Salford, England, asks the question “Do you shake hands with mothers of floppy babies?” as the title to his article on congenital myotonic dystrophy. [2]

Language: English
Page range: 29 - 30
Published on: Sep 1, 1987
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services

© 1987 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.