Craniofacial fibrous dysplasia: Clinical characteristics and long-term outcomes

Eye

Volumn 23, Issue 12, 2009, Pages 2175-2181

  Rahman, A M A ^a,b   Madge, S N ^a,b   Billing, K ^a,b   Anderson, P J ^c   Leibovitch, I ^d   Selva, D ^a,b   David, D ^c  

^a UNIVERSITY OF ADELAIDE   (Australia)

^b Hanson Institute   (United States)

^c North Adelaide SA   (United States)

^d TEL AVIV UNIVERSITY   (Israel)

Author keywords

Fibrous dysplasia; Optic canal decompression; Optic neuropathy

Indexed keywords

ADULT; ALBRIGHT SYNDROME; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CRANIOFACIAL FIBROUS DYSPLASIA; FEMALE; FIBROUS DYSPLASIA; FOLLOW UP; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LONG TERM CARE; MALE; OUTCOME ASSESSMENT; VISUAL ACUITY;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; EYE DISEASES; FACIAL BONES; FEMALE; FIBROUS DYSPLASIA OF BONE; HUMANS; INFANT; LONGITUDINAL STUDIES; MALE; MIDDLE AGED; POSTOPERATIVE COMPLICATIONS; RETROSPECTIVE STUDIES; SKULL; TOMOGRAPHY, X-RAY COMPUTED; VISION DISORDERS; VISUAL ACUITY; YOUNG ADULT;

EID: 72749113316     PISSN: 0950222X     EISSN: 14765454     Source Type: Journal    
DOI: 10.1038/eye.2009.6     Document Type: Article

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