Non-ossifying fibroma, fibrous cortical defect and Jaffe-Campanacci syndrome: a biologic and clinical review.

La Chirurgia degli organi di movimento

Volumn 93, Issue 1, 2009, Pages 1-7

  Mankin, Henry J ^a   Trahan, Carol A ^b   Fondren, Gertrud ^b   Mankin, Carole J ^b  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ALBRIGHT SYNDROME; AXILLA; BONE TUMOR; CAFE AU LAIT SPOT; CHILD; DERMATOFIBROMA; DIFFERENTIAL DIAGNOSIS; FEMALE; HUMAN; INFANT; MALE; MELANOSIS; MENTAL DEFICIENCY; MIDDLE AGED; NEUROFIBROMATOSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGIC FRACTURE; PATHOLOGY; PHENOTYPE; PRESCHOOL CHILD; REGISTER; REVIEW; SYNDROME;

ADOLESCENT; ADULT; AGED; AXILLA; BONE NEOPLASMS; CAFE-AU-LAIT SPOTS; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; FRACTURES, SPONTANEOUS; HISTIOCYTOMA, BENIGN FIBROUS; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; MELANOSIS; MENTAL RETARDATION; MIDDLE AGED; NEUROFIBROMATOSIS 1; PHENOTYPE; REGISTRIES; SYNDROME; YOUNG ADULT;

EID: 79959334312     PISSN: None     EISSN: 19732538     Source Type: Journal    
DOI: 10.1007/s12306-009-0016-4     Document Type: Review

References (62)