Sklower Brooks S, Kassner G, Qazi Q, Keogh M J, Gorlin R J
NYS Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Am J Med Genet. 1996 Dec 11;66(2):154-62. doi: 10.1002/(SICI)1096-8628(19961211)66:2<154::AID-AJMG6>3.0.CO;2-R.
We report on a boy with clinical and radiologic findings of osteoglophonic dysplasia. He had craniostenosis, "bizarre," expansile cystic lesions in the diaphyses, delayed tooth eruption, and progressive rib expansion typical of the syndrome. Initially delayed psychomotor development with later normal intelligence, early feeding and breathing difficulty, and speech delay are also characteristic of the disorder. Manifestations, not previously reported in osteoglophonic dysplasia, present in the propositus are spontaneous fractures resulting in pseudoarthroses through cystic and dysplastic foci in his proximal femoral shafts and right humerus, pretibial dimples, hypospadias, marked rib expansion, and absence of significant vertebral abnormality. These findings expand the spectrum of osteoglophonic dysplasia.
我们报告了一名患有骨肥厚性发育异常的临床和放射学表现的男孩。他有颅骨狭窄、骨干中“奇异的”膨胀性囊性病变、牙齿萌出延迟以及该综合征典型的进行性肋骨增宽。最初精神运动发育迟缓,后来智力正常,早期喂养和呼吸困难以及语言发育迟缓也是该疾病的特征。先证者出现了骨肥厚性发育异常中以前未报道过的表现,即通过股骨近端骨干和右肱骨中的囊性和发育异常病灶导致假关节形成的自发性骨折、胫前酒窝、尿道下裂、明显的肋骨增宽以及无明显的椎体异常。这些发现扩展了骨肥厚性发育异常的范围。