Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with Klippel-Feil syndrome: Clues from the BMP signaling pathway

Spine

Volumn 30, Issue 12, 2005, Pages 1379-1385

  Schaffer, Alyssa A ^a   Kaplan, Frederick S ^b,d   Tracy, Michael R ^a   O'Brien, Megan L ^a   Dormans, John P ^a,b   Shore, Eileen M ^b   Harland, Richard M ^b   Kusumi, Kenro ^a,c  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Bone morphogenetic protein pathway; Cervical spine; Fibrodysplasia ossificans progressiva; Heterotopic ossification; Klippel Feil; Noggin

Indexed keywords

BONE MORPHOGENETIC PROTEIN; NOGGIN;

ADOLESCENT; ADULT; CERVICAL SPINE; CHILD; CLINICAL FEATURE; CONNECTIVE TISSUE; CONTROLLED STUDY; DISEASE COURSE; DISEASE SEVERITY; EMBRYO SEGMENTATION; FEMALE; GENE DELETION; GENE MUTATION; HOMOZYGOSITY; HUMAN; KLIPPEL FEIL SYNDROME; MAJOR CLINICAL STUDY; MALE; METAMORPHOSIS; OSSIFYING MYOSITIS; PATHOGENESIS; PRIORITY JOURNAL; REVIEW; SIGNAL TRANSDUCTION; SPINE FUSION; SPINE MALFORMATION; SPINE RADIOGRAPHY; VERTEBRA BODY;

ADOLESCENT; ADULT; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; CERVICAL VERTEBRAE; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; INFANT; KLIPPEL-FEIL SYNDROME; MALE; MICE; MIDDLE AGED; MUSCLE RIGIDITY; MYOSITIS OSSIFICANS; RANGE OF MOTION, ARTICULAR; SIGNAL TRANSDUCTION;

EID: 25844529319     PISSN: 03622436     EISSN: 15281159     Source Type: Journal    
DOI: 10.1097/01.brs.0000166619.22832.2c     Document Type: Review

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