Dysorders with Defective Mineralization

J. Spranger, P. Brill, C. Hall, G. Nishimura, A. Superti-Furga, S. Unger
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Abstract

This chapter further discusses bone dysplasias and includes discussion on hypophosphatasia, neonatal severe primary hyperparathyroidism, and hereditary rickets. Each discussion includes major radiographic features, major clinical findings, major laboratory findings, genetics, major differential diagnoses, and a bibliography.
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本章进一步讨论骨发育不良,包括对磷酸酶低下、新生儿严重原发性甲状旁腺功能亢进和遗传性佝偻病的讨论。每个讨论包括主要的放射学特征,主要的临床发现,主要的实验室发现,遗传学,主要的鉴别诊断和参考书目。
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