Title of article
Jaffe-Campanacci Syndrome Report of a Case
Author/Authors
Torabi Nezhad, S Department of Pathology - Shiraz University of medical sciences , Nooraie, H Department of Orthopedics - Shiraz University of medical sciences , Arshadi, C Department of Radiology - Shiraz University of medical sciences Corresponding Author Dr S. Torabi Nezhad Department of Pathology - Shiraz university of Medical Sciences, Shiraz , Mohseni, A Department of Pathology - Shiraz University of medical sciences , Dehghani, F Department of Orthopedics - Shiraz University of medical sciences
Pages
4
From page
63
To page
66
Abstract
I am reporting a 7-year old boy presenting with multiple non-ossifying fibromas and associated extraskeletal congenital anomalies. such as cataract–café - au- lait spots. hypogonadism, cataract and cardiovascular malformation. Review of the clinical features and correlation with pathologic and radiologic data support a diagnosis Jaffe-Campanacci syndrome; a rare malformation syndrome, possibly related to neurofibromatosis.
Index Terms: skeletal anomalies, Non ossifying fibroma, (nof), fibrous cortical defect (FCD) ,
Keywords
non ossifying fibroma , neurofibromatosis
Journal title
Astroparticle Physics
Serial Year
2003
Record number
2434861
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