Winter R M, Patton M A, Challener J, Mueller R F, Baraitser M
Kennedy Galton Centre, Northwick Park Hospital, London.
J Med Genet. 1989 May;26(5):320-5. doi: 10.1136/jmg.26.5.320.
Four unrelated patients are reported with short stature, stiffness of the joints, short fingers, inability to make a fist, and thickened skin on the forearms. Investigations have failed to show a lysosomal storage disorder and radiographs show non-specific changes with a delayed carpal bone age. The clinical features in the four children are very similar to the recently described acromicric dysplasia. There are also similarities to Moore-Federman syndrome which has only been described in one family. The case is made that acromicric dysplasia and Moore-Federman syndrome are the same entity.
报告了4例无血缘关系的患者,他们身材矮小、关节僵硬、手指短小、无法握拳且前臂皮肤增厚。检查未发现溶酶体贮积症,X线片显示非特异性改变且腕骨年龄延迟。这4名儿童的临床特征与最近描述的肢端短小发育不良非常相似。与仅在一个家族中被描述过的穆尔-费德曼综合征也有相似之处。有理由认为肢端短小发育不良和穆尔-费德曼综合征是同一病症。