Scott-Emuakpor A B, Heffelfinger J, Higgins J V
Am J Dis Child. 1977 Feb;131(2):167-9. doi: 10.1001/archpedi.1977.02120150049010.
We describe a syndrome of microcephaly, with extreme failure to thrive, (severe spasticity), kyphoscollosis, cataracts, and hip dysplasia in four siblings. The syndrome could be a new one, although it has several features resembling those described by Lowry et al. It is suggested that this syndrome is inherited as an autosomal-recessive condition.
我们描述了一种综合征,该综合征在四个兄弟姐妹中表现为小头畸形、极度生长发育迟缓、(严重痉挛)、脊柱后凸侧弯、白内障和髋关节发育不良。尽管该综合征有几个特征与洛瑞等人描述的相似,但它可能是一种新的综合征。有人认为这种综合征是以常染色体隐性方式遗传的。