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10.1097/BPO.0b013e318220396e

http://scihub22266oqcxt.onion/10.1097/BPO.0b013e318220396e
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21654472!ä!21654472

suck abstract from ncbi

pmid21654472      J+Pediatr+Orthop 2011 ; 31 (5): 599-605
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  • Orthopaedic conditions in Ras/MAPK related disorders #MMPMID21654472
  • Reinker KA; Stevenson DA; Tsung A
  • J Pediatr Orthop 2011[Jul]; 31 (5): 599-605 PMID21654472show ga
  • BACKGROUND: The RAS/MAPK disorders [Noonan syndrome, cardiofaciocutaneous (CFC) syndrome, Costello syndrome, and Leopard syndrome] are heterogenous conditions with phenotypic overlap. Their orthopaedic manifestations are not well defined, and their phenotypic similarity makes differentiating them difficult. METHODS: We prospectively evaluated 60 individuals: 26 with Noonan syndrome, 32 with CFC syndrome, and 2 with Costello syndrome. Each individual underwent a structured orthopaedic history and physical evaluation by an orthopaedic surgeon, and a syndromic evaluation by a geneticist. RESULTS: All groups had a high prevalence of scoliosis (8/26 Noonan syndrome, 8/32 CFC syndrome, and 1/2 Costello). Those with Noonan syndrome or CFC syndrome had a high instance of serious cervical spine disorders, including cervical stenosis, Arnold-Chiari malformation, and syringomyelia in the Noonan syndrome individuals and hydrocephalus, cervical stenosis, torticollis, and Arnold-Chiari in the CFC syndrome individuals. Noonan syndrome manifestations included chronic pain (n=21), pes planus (n=11), pes cavus (n=5), hip contractures (n=5), hand dysfunction (n=3), and hip dysplasia (n=2). Manifestations of CFC syndrome included pes planovalgus (n=20), knee flexion contractures (n=7), hip dysplasia (n=5), elbow flexion contractures (n=4), pedal calluses (n=4), toe crowding (n=4), and hip contractures (n=4). Individuals with Costello syndrome had shorter stature than the other groups and were prone to have hand contractures. CONCLUSIONS: Orthopaedic manifestations are frequent and diverse in Ras/MAPK disorders and can be used in phenotypic differentiation between these disorders. LEVEL OF EVIDENCE: II.
  • |Abnormalities, Multiple/genetics[MESH]
  • |Adolescent[MESH]
  • |Arnold-Chiari Malformation/*complications/genetics[MESH]
  • |Child[MESH]
  • |Child, Preschool[MESH]
  • |Ectodermal Dysplasia/*complications/genetics[MESH]
  • |Facies[MESH]
  • |Failure to Thrive/*complications/genetics[MESH]
  • |Female[MESH]
  • |Genes, ras/*genetics[MESH]
  • |Heart Defects, Congenital/*complications/genetics[MESH]
  • |Humans[MESH]
  • |Incidence[MESH]
  • |Infant[MESH]
  • |LEOPARD Syndrome/*complications/genetics[MESH]
  • |MAP Kinase Signaling System/*genetics[MESH]
  • |Male[MESH]
  • |Musculoskeletal Diseases/epidemiology/*etiology/genetics[MESH]
  • |Mutation[MESH]
  • |Noonan Syndrome/*complications/genetics[MESH]
  • |Protein Tyrosine Phosphatase, Non-Receptor Type 11/genetics[MESH]
  • |Risk Factors[MESH]


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