Insights Into Management of Camurati-Engelmann Disease: A Case Series of Three Siblings

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Angioid streaks in a case of Camurati–Engelmann disease

Camurati-Engelmann disease (CED) is a rare autosomal dominant disease with various phenotypic expressions. The hallmark of the disease is bilateral symmetric diaphyseal hyperostosis of the long bones with progressive involvement of the metaphysis. Ocular manifestations occur rarely and mainly result from bony overgrowth of the orbit and optic canal stenosis. We report a case of CED showing angi...

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Skull base manifestations of Camurati-Engelmann disease.

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Imaging aspects of Camurati-Engelmann disease.

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ژورنال

عنوان ژورنال: International Journal of Clinical Pediatrics

سال: 2020

ISSN: 1927-1255,1927-1263

DOI: 10.14740/ijcp403