A Case of Congenital Myotonic Dystrophy.
- Author:
Taek Jin LEE
1
;
Kyung Sik KIM
;
Ran NAMGUNG
;
Kook In PARK
;
Chul LEE
;
Young Mock LEE
;
Jin Sung LEE
;
Tae Seung KIM
Author Information
1. Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea. ranng@yumc.yonsei.ac.kr
- Publication Type:Case Report
- Keywords:
Congenital myotonic dystrophy;
Hypotonia;
Respiratory insufficiency;
Newborn
- MeSH:
Arthrogryposis;
Gestational Age;
Humans;
Infant, Newborn;
Infant, Premature;
Mothers;
Muscle Hypotonia;
Muscle Weakness;
Myotonic Dystrophy*;
Parturition;
Polyhydramnios;
Respiratory Insufficiency
- From:Journal of the Korean Society of Neonatology
2002;9(2):204-210
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Congenital myotonic dystrophy is an almost always maternally-inherited autosomal dominant multisystem disorder of variable clinical expressions characterized by hypotonia and frequent respiratory distress at birth. The muscle weakness may be so severe, it may lead to death in the newborn period. We report a case of congenital myotonic dystrophy in a 34 weeks of gestational age premature infant born to a mother with polyhydramnios, presenting with hypotonia, respiratory insufficiency, feeding difficulties and arthrogryposis. A brief review of literature is given.
