Infantile scoliosis in Marfan syndrome

Paul D. Sponseller, Navin Sethi, Duke E. Cameron, Reed E. Pyeritz

Research output: Contribution to journalArticle

Abstract

Study Design. A retrospective review of clinical data was conducted. Objectives. To determine the characteristics of infantile scoliosis in Marfan syndrome and the response to treatment of patients with this condition. Summary of Background Data. No previous study has reported the features of this condition nor the effect of treatment on patients with this syndrome. Methods. The data on all patients seen at one institution who had Marfan syndrome and scoliosis by age three were reviewed. Fourteen of the 600 patients from the group examined who had Marfan syndrome fit the above criteria. Skeletal and general features were studied. Results. Thirteen of the 14 patients had no family history of Marfan syndrome, a finding which does not fit the usual autosomal dominant inheritance pattern. All 14 patients had exaggeration of the Marfan. All but one patient had cardiac valvular insufficiency that required repair by age 11. Thirteen patients had thoracic aortic aneurysm, 10 had lens dislocation, and eight had sternal deformity. Three patients had hip dislocations, two had pyloric stenosis, and two had dural ectasia. Motor delay was evidenced by onset of walking past 18 months in nine patients; three of these patients were never able to walk independently. One patient each died at ages 1, 3, 4, and 8 years; all others have survived to present (mean age, 13 years). The mean curve of the patients' spines at presentation was 38°. Eleven curves were double major, two were thoracolumbar, and one was double thoracic. Brace wear did not halt curve progression in any of the nine patients for whom it was used. Instrumentation without fusion was used in three patients for a mean of 3 years, with best results in one nonkyphotic curve. Nine patients underwent instrumented fusion at a mean age of 6.6 years (range, 3-13 years). Mean curve correction was 51% (from 72°to 34°). Final mean curve was 54°for a mean correction of 20% at the 5-year (average, 5.4 years) follow-up examination. Acute complications occurred in three patients, and five patients needed a second surgery for late complications. Causes for curve increase after surgery included growth and loss of fixation. Conclusions. In this most severe form of Marfan syndrome, bracing has a limited role and is only to be used if the curve is less than 40°. Surgery should not be performed on a patient younger than four years of age because many patients with large curves before this age will succumb spontaneously to cardiac complications. Instrumentation without fusion should be considered only for patients with no significant kyphosis. Results of fusion are better for patients who are older than five years of age.

Original languageEnglish (US)
Pages (from-to)509-516
Number of pages8
JournalSpine
Volume22
Issue number5
DOIs
StatePublished - Mar 1 1997

Keywords

  • Marfan syndrome
  • infantile scoliosis

ASJC Scopus subject areas

  • Orthopedics and Sports Medicine
  • Clinical Neurology

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    Sponseller, P. D., Sethi, N., Cameron, D. E., & Pyeritz, R. E. (1997). Infantile scoliosis in Marfan syndrome. Spine, 22(5), 509-516. https://doi.org/10.1097/00007632-199703010-00008