Cohen M M, Gorlin R J
Department of Oral Biology, Faculty of Dentistry, Dalhousie University, Halifax, Nova Scotia, Canada.
Am J Med Genet. 1991 Jun 1;39(3):332-5; discussion 336-7. doi: 10.1002/ajmg.1320390316.
We have coined the term "pseudo-trisomy 13 syndrome" to designate cases of holoprosencephaly, severe facial anomalies, postaxial polydactyly, various other congenital defects, and normal chromosomes. Eleven instances are summarized. Two pairs of sibs and two other cases with consanguinity suggest autosomal recessive inheritance. Autosomal recessive inheritance is possible. Alternately, an undetected microdeletion and etiologic heterogeneity (some cases possibly representing dominant new mutations) must be considered. Further delineation is necessary. It is hoped that this paper will serve as a focus for further discussion of the problem.
我们创造了“假三体13综合征”这一术语,用于指代全前脑畸形、严重面部异常、轴后多指畸形、各种其他先天性缺陷且染色体正常的病例。总结了11个病例。两对同胞以及另外两例有血缘关系的病例提示为常染色体隐性遗传。常染色体隐性遗传是有可能的。另外,必须考虑未被检测到的微缺失和病因异质性(某些病例可能代表显性新突变)。需要进一步明确。希望本文能成为对该问题进行进一步讨论的焦点。