Le Merrer M, Briard M L, Chauvet M L
J Genet Hum. 1987 May;35(2-3):187-93.
The authors report three cases of a new syndrome which characteristic anomalies are facial dysmorphism with anteverted nose, down slanting palpebral fissures, ptosis, severe microretrognatia, polydactyly. The authors insist on the particular severe genital anomalies, the failure to thrive and the constant lethal issue. The authors discuss the diagnosis of Smith-Lemli-Opitz syndrome and suggest the possibility of a new entity always confounded with others associations characterized by a polydactyly and a sexual reversion in male.
作者报告了三例一种新综合征的病例,其特征性异常包括面部畸形(鼻前倾、睑裂向下倾斜、上睑下垂、严重小下颌后缩)、多指畸形。作者强调了特别严重的生殖器异常、生长发育迟缓以及持续的致命问题。作者讨论了史密斯-勒米-奥皮茨综合征的诊断,并提出了一种新实体的可能性,该实体总是与其他以多指畸形和男性性反转特征的综合征相混淆。