Shebib S, Hugosson C, Sakati N, Nyhan W L
Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Am J Med Genet. 1991 Aug 1;40(2):146-50. doi: 10.1002/ajmg.1320400205.
A patient with intrauterine growth retardation and marked postnatal retardation of growth had microcephaly and the orofacial and dental characteristics of the Seckel phenotype. In addition she had short forearms, metaphyseal flare, especially of the distal femora, triangular distal femoral epiphyses, and pseudoepiphyses of the hands, all characteristics of an osteodysplastic variant. Parental consanguinity suggests autosomal recessive inheritance.
一名患有宫内生长迟缓及出生后明显生长发育迟缓的患者,有小头畸形以及塞克尔综合征的口面部和牙齿特征。此外,她还有前臂短小、干骺端增宽(尤其是股骨远端)、股骨远端骨骺呈三角形以及手部假骨骺,这些都是骨发育异常变体的特征。父母近亲结婚提示为常染色体隐性遗传。