Respiratory deterioration during growth hormone therapy in a case of congenital nemaline myopathy.
作者信息
Logghe K, Wit J M, Jennekens F, Pruijs J E
机构信息
Department of Paediatrics, University Hospital for Children and Youth, Het Wilhelmina Kinderziekenhuis, Utrecht, The Netherlands.
出版信息
Eur J Pediatr. 1990 Nov;150(1):69-71. doi: 10.1007/BF01959486.
PMID:2079082
Abstract
Congenital nemaline myopathy (CNM) is generally classified as a non-progressive or slowly progressive neuromuscular disease. We describe a boy with CNM and an isolated partial growth hormone (GH) deficiency. From the onset of GH therapy his respiratory capacity deteriorated rapidly. The possible association between this deterioration and GH therapy is discussed.
摘要
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