Heiman-Patterson T D, Rosenberg H R, Binning C P, Tahmoush A J
Department of Neurology, Hahnemann University Hospital, Philadelphia, PA 19102.
Pediatr Neurol. 1986 May-Jun;2(3):175-7. doi: 10.1016/0887-8994(86)90013-5.
The King-Denborough syndrome (KDS) is characterized by dysmorphic features, myopathy, and malignant hyperthermia (MH). Physiologic contracture testing for MH susceptibility has not been reported in KDS. A young boy with KDS underwent muscle biopsy evaluation at age 3 years that documented an abnormal contracture response to halothane, indicating MH susceptibility. Histopathology demonstrated small type II fibers associated with type I hypertrophy. Contracture testing of muscle obtained from the patient's mother was positive, while a sibling's test was negative. This case is the first to demonstrate susceptibility to MH with KDS by using physiologic contracture testing. The presence of positive MH results in both the patient and his mother suggest one of the following: (1) KDS may be part of the spectrum of autosomal dominantly inherited MH; (2) the locus for MH and for KDS may be linked closely and inherited concurrently, or; (3) the association of MH and KDS may be coincidental.
金-丹伯勒综合征(KDS)的特征为畸形体征、肌病和恶性高热(MH)。尚未有关于KDS患者进行MH易感性生理挛缩试验的报道。一名患有KDS的小男孩在3岁时接受了肌肉活检评估,结果显示其对氟烷的挛缩反应异常,表明存在MH易感性。组织病理学显示存在小型II型纤维并伴有I型纤维肥大。对患者母亲的肌肉进行挛缩试验结果为阳性,而其一名兄弟姐妹的试验结果为阴性。该病例是首例通过生理挛缩试验证实KDS患者存在MH易感性的病例。患者及其母亲的MH结果均为阳性提示以下情况之一:(1)KDS可能是常染色体显性遗传MH谱系的一部分;(2)MH和KDS的基因座可能紧密连锁并同时遗传,或者;(3)MH与KDS之间的关联可能是巧合。