Tüysüz Beyhan, Ungür Savaş
Department of Pediatrics, Cerrahpaşa Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Am J Med Genet A. 2003 Jun 15;119A(3):375-80. doi: 10.1002/ajmg.a.20125.
We present a 27-year-old girl with short trunk stature, generalized rectangular platyspondyly and strike precocious calcification of costal cartilage. She had also brachydactyly, small nails, strabismus and delay of menarche. Her 16-year-old sister had also short trunk stature with severe kyphoscoliosis, hearing loss, brachydactyly, platyspondyly and mild precocious calcification of costal cartilages. Their 12-year-old brother had short trunk stature, kyphoscoliosis, brachydactyly, and platyspondyly but did not show precocious calcification of costal cartilage. The patients shared the following features: short trunk stature, brachydactyly, severe rectangular platyspondyly, broad and short femoral necks and hypoplasia of the ileum. In addition, the older sister had strike precocious calcification of costal cartilage while her sister and brother had severe kyphoscoliosis. Although short trunk stature and severe rectangular platyspondyly without significant epiphyseal or metaphyseal changes were in favor of Hobaek type brachyolmia, this diagnosis was not considered, both because, there were no specific radiological findings of this syndrome, such as elongated vertebral bodies extending beyond the pedicles laterally and all of the patients had brachydactyly which was not present in Hobaek type brachyolmia. The parents were healthy and first cousins signifying autosomal recessive inheritance. We considered that the patients could be affected by a new distinct autosomal recessive type brachyolmia or a new skeletal dysplasia.
我们报告一名27岁女性,身材短躯干,全身普遍性扁平椎,肋软骨显著早熟钙化。她还患有短指畸形、小指甲、斜视和初潮延迟。她16岁的姐姐同样身材短躯干,伴有严重脊柱侧凸后凸、听力丧失、短指畸形、扁平椎以及肋软骨轻度早熟钙化。她们12岁的弟弟身材短躯干,有脊柱侧凸后凸、短指畸形和扁平椎,但未表现出肋软骨早熟钙化。这些患者有以下共同特征:身材短躯干、短指畸形、严重的长方形扁平椎、股骨颈宽短以及回肠发育不全。此外,姐姐有显著的肋软骨早熟钙化,而她的妹妹和弟弟有严重的脊柱侧凸后凸。尽管身材短躯干和严重的长方形扁平椎且无明显骨骺或干骺端改变支持霍贝克型短躯干侏儒症,但未考虑该诊断,原因在于,此综合征无特异性影像学表现,如椎体向外侧延伸超过椎弓根,且所有患者均有短指畸形,而霍贝克型短躯干侏儒症不存在此情况。父母健康,为近亲结婚,提示常染色体隐性遗传。我们认为这些患者可能患有一种新的独特的常染色体隐性型短躯干侏儒症或一种新的骨骼发育不良。