Orthopaedic conditions in Ras/MAPK related disorders

J Pediatr Orthop. 2011 Jul-Aug;31(5):599-605. doi: 10.1097/BPO.0b013e318220396e.

Abstract

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.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics
  • Adolescent
  • Arnold-Chiari Malformation / complications*
  • Arnold-Chiari Malformation / genetics
  • Child
  • Child, Preschool
  • Ectodermal Dysplasia / complications*
  • Ectodermal Dysplasia / genetics
  • Facies
  • Failure to Thrive / complications*
  • Failure to Thrive / genetics
  • Female
  • Genes, ras / genetics*
  • Heart Defects, Congenital / complications*
  • Heart Defects, Congenital / genetics
  • Humans
  • Incidence
  • Infant
  • LEOPARD Syndrome / complications*
  • LEOPARD Syndrome / genetics
  • MAP Kinase Signaling System / genetics*
  • Male
  • Musculoskeletal Diseases / epidemiology
  • Musculoskeletal Diseases / etiology*
  • Musculoskeletal Diseases / genetics
  • Mutation
  • Noonan Syndrome / complications*
  • Noonan Syndrome / genetics
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics
  • Risk Factors
  • United States / epidemiology

Substances

  • Protein Tyrosine Phosphatase, Non-Receptor Type 11

Supplementary concepts

  • Cardiofaciocutaneous syndrome