Fryns J P, Van Den Berghe H
Center for Human Genetics, University of Leuven, Belgium.
Genet Couns. 1991;2(4):241-4.
In this report, we present two further examples of X-linked mental retardation with Marfanoid habitus. Follow-up data on these two patients reveal that the clinical diagnosis of this syndrome is extremely difficult, if not impossible before puberty, as the Marfanoid habitus only becomes strikingly evident during adolescence.
在本报告中,我们展示了另外两个患有马凡氏体型的X连锁智力障碍的病例。对这两名患者的随访数据显示,该综合征的临床诊断极其困难,在青春期前即便不是不可能,也很难做出诊断,因为马凡氏体型在青春期才会变得极为明显。