Korinthenberg R, Palm D, Schlake W, Klein J
Eur J Pediatr. 1984 Apr;142(1):64-8. doi: 10.1007/BF00442595.
We report on two brothers and an unrelated girl with congenital muscular dystrophy (CMD), brain malformation and ocular changes (strabismus, myopia, glaucoma, cataracts, retinal dystrophy). Correlations with the inherited autosomal recessive syndromes of CMD, including the Fukuyama-type CMD with CNS malformation, and the Muscle, Eye and Brain Disease published by Santavuori are discussed.
我们报告了两名患有先天性肌营养不良(CMD)、脑畸形和眼部病变(斜视、近视、青光眼、白内障、视网膜营养不良)的兄弟以及一名无血缘关系的女孩。文中讨论了这些症状与遗传性常染色体隐性CMD综合征的关联,包括伴有中枢神经系统畸形的福山型CMD,以及Santavuori发表的肌肉、眼睛和脑部疾病。