Hajdu-Cheney综合征:一种罕见的肢端溶骨症

IF 0.1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING West African Journal of Radiology Pub Date : 2018-07-01 DOI:10.4103/WAJR.WAJR_3_18

M. Olusola-Bello, A. Olatunji, O. Toyobo

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摘要

我们报告一例35岁的妇女患有Hajdu-Cheney综合征，这是一种非常罕见的结缔组织疾病，自1948年以来，全世界约有70例报告。家族中未见类似疾病。她表现出该综合征的临床特征，并在几次牙科手术后留下第七脑神经麻痹。颅骨和手的x线片清楚地显示了异常。

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Hajdu–Cheney syndrome: A rare acro-osteolytic disorder

We report a case of a 35-year-old woman with Hajdu–Cheney syndrome, a very rare connective tissue disorder with about 70 cases reported worldwide since 1948. No similar disease occurred in her family. She presented with clinical features of the syndrome and left seventh cranial nerve palsy after several dental procedures. The radiographs of the skull and the hands demonstrate the abnormalities clearly.

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West African Journal of Radiology RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-

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