Van Maldergem L, Gillerot Y, Perlmutter N, Wetzburger C, Koulischer L
Centre de Génétique Humaine, Institut de Morphologie Pathologique, Loverval, Belgium.
Am J Med Genet. 1990 Oct;37(2):283-5. doi: 10.1002/ajmg.1320370225.
A 21-year-old male with mental retardation, short stature, almond-shaped eyes, small downturned mouth, and coned epiphyses is presented. The clinical presentation, as well as the metacarpal phalangeal pattern profile, was similar to the affected members of a family reported by Hunter et al.: (Hunter et al.: J Med Genet 14:430-437, 1977). In addition, many features of our patient resembled Ruvalcaba syndrome. However, skeletal abnormalities were different. A reciprocal translocation was also observed in 3 members of our patient's family.
报告了一名21岁男性,有智力发育迟缓、身材矮小、杏仁状眼、嘴角下斜及骨骺呈锥形。其临床表现以及掌指骨模式轮廓与Hunter等人报告的一个家族中受影响成员相似(Hunter等人:《医学遗传学杂志》14:430 - 437,1977年)。此外,我们患者的许多特征类似于Ruvalcaba综合征。然而,骨骼异常有所不同。在我们患者家族的3名成员中还观察到了相互易位。