Seminars in Pediatric Surgery
Volume 17, Issue 3 , Pages 167-172, August 2008

Jeune's syndrome (asphyxiating thoracic dystrophy): congenital and acquired

  • J. Duncan Phillips, MD

      Affiliations

    • Division of Pediatric Surgery, School of Medicine, University of North Carolina, Chapel Hill, North Carolina
    • Corresponding Author InformationAddress reprint requests and correspondence: J. Duncan Phillips, MD, 3010 Old Clinic Building, CB #7223, Chapel Hill, NC 27599.
  • ,
  • John A. van Aalst, MD

      Affiliations

    • Division of Plastic Surgery, School of Medicine, University of North Carolina, Chapel Hill, North Carolina.

Familial asphyxiating thoracic dystrophy (ATD), also known as Jeune's syndrome, is a rare autosomal recessive disorder with variable severity and multiple musculo-skeletal manifestations. Respiratory distress may be severe, resulting in death during infancy. Surgical repair techniques have typically involved median sternotomy (with graft interposition), resulting in poor outcomes. Acquired ATD may rarely result from impairment of chest wall growth following “open” (Ravitch-type) repair of pectus excavatum or carinatum deformities. Symptomatic patients may have profound restriction of pulmonary function. Repair techniques typically involve re-do Ravitch-type procedures or median sternotomy with rib graft interposition. Mild to moderate improvements in pulmonary function tests have been documented.

Keywords: Asphyxiating thoracic dystrophy, Jeune's syndrome, Pectus excavatum, Pectus carinatum, Asphyxiating thoracic dysplasia

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PII: S1055-8586(08)00015-2

doi:10.1053/j.sempedsurg.2008.03.006

Seminars in Pediatric Surgery
Volume 17, Issue 3 , Pages 167-172, August 2008