Abstract
In a case of myotonic dystrophy, discovered during childhood, peristalsis of the esophagus has been found to be abnormal in spite of paucity of clinical signs. Anomalous motility of its upper part and significantly depressed pressure in the lower segment, as shown by manometry, have been correlated with radiological abnormalities.
References
Aicardi J (1975) Clinical and genetic aspects of the early forms of Steinert's dystrophia myotonica. J Genet Hum 23: 146
Bell DB, Smith DW (1972) Myotonic dystrophy in the neonate. J Pediatr 4: 81
Dobowitz V (1978) Muscles disorders in childhood. Saunders, Philadelphia London Toronto, p 135
Lenard HG, Goebel HH, Weigel W (1977) Smooth muscle involvement in congenital myotonic dystrophy. Neuropaediatric 8: 48
Piffaretti PG (1966) Les troubles de la mobilité pharyngo-oesophagienne dans la maladie de Steinert. Gastroenterologia 106: 97
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Mabille, J.P., Giroud, M. & Athias, P. Esophageal involvement in a case of congenital myotonic dystrophy. Pediatr Radiol 12, 89–91 (1982). https://doi.org/10.1007/BF00972440
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DOI: https://doi.org/10.1007/BF00972440