Lomboni L, Baccichetti Y, Mokdad R, Dandine M, Tassy R, Eliachar E, Molhant G
Rev Stomatol Chir Maxillofac. 1984;85(6):501-4.
A one year old child with Kniest's disease was admitted for reconstructive surgery of the bone deficit of a palatine cleft. This syndrome is recognizable at a very early age by the shortness of the limbs or the increase in size of the joints. Clinically it associates mild facial dystrophy and nanism from reduction in height of the trunk and the shortness and deviations of the limbs. Frequently associated are myopia, deafness and a palatine cleft. Radiological signs are reduced height of vertebral bodies, and a not infrequent finding is a cuneiform deformity of the first lumbar vertebrae. Epiphyseal development is anarchic, that of the knee large, while the femoral head is small, fragmented or absent. Transmission is by the dominant mode. Kniest's syndrome must be differentiated from metratropic dwarfism in which there is greater progression of spinal deformities.
一名患有克尼斯特病的1岁儿童因腭裂骨缺损修复手术入院。这种综合征在很小的时候就可以通过四肢短小或关节增大来识别。临床上,它伴有轻度面部发育不良以及由于躯干高度降低、四肢短小和畸形导致的侏儒症。常见的伴随症状有近视、耳聋和腭裂。放射学表现为椎体高度降低,第一腰椎楔形畸形也不少见。骨骺发育紊乱,膝关节骨骺大,而股骨头小、破碎或缺失。遗传方式为显性遗传。克尼斯特综合征必须与椎体骨骺发育不良性侏儒症相鉴别,后者脊柱畸形进展更严重。