一例罕见的致密性骨发育不全病例。
An unusual case of pycnodysostosis.
作者信息
Kumar R, Misra P K, Singhal R
机构信息
Department of Paediatrics, King George's Medical College, Lucknow, India.
出版信息
Arch Dis Child. 1988 May;63(5):558-9. doi: 10.1136/adc.63.5.558.
Abstract
A 6 year old boy with clinical and radiological features of pycnodysostosis is described. In addition to pycnodysostosis he had a myelophthisic type of anaemia suggesting an overlap with osteopetrosis.
摘要
描述了一名患有致密性成骨不全临床和放射学特征的6岁男孩。除致密性成骨不全外，他还患有骨髓痨型贫血，提示与骨硬化症有重叠。
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本文引用的文献
1
Pycnodysostosis, with a familial chromosome anomaly.致密性骨发育不全，伴家族性染色体异常。
Am J Med. 1966 Feb;40(2):273-82. doi: 10.1016/0002-9343(66)90108-2.
2
Tetracycline-based study of bone dynamics in pycnodysostosis.基于四环素的致密性骨发育不全骨动力学研究。
Clin Orthop Relat Res. 1971 Jan;74:301-12. doi: 10.1097/00003086-197101000-00035.
3
Pycnodysostosis. A variant form with visceral manifestations.致密性骨发育不全。一种伴有内脏表现的变异型。
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4
Plasma calcitonin in pycnodysostosis: intermittently high basal levels and exaggerated responses to calcium and glucagon infusions.致密性成骨不全症中的血浆降钙素：基础水平间歇性升高以及对钙和胰高血糖素输注反应过度。
J Clin Endocrinol Metab. 1973 Jul;37(1):46-55. doi: 10.1210/jcem-37-1-46.
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