Ehlers-Danlos Syndrome and Congenital Heart Anomalies.

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  • MAEDA Toyoki
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University
  • SUZUKI Yasuyo
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University
  • HAENO Shigehiko
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University
  • ASADA Midori
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University
  • HIRAMATSU Ryouji
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University
  • TANAKA Fumiaki
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University
  • OKADA Masaji
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University
  • SUZUKI Tomokazu
    The Department of Clinical Genetics, Institute of Bioregulation, Kyushu University

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Two sisters with Ehlers-Danlos syndrome, inherited as an autosomal recessive trait, and congenital heart disease are herein reported. One was a 20-year-old woman with Ehlers-Danlos syndrome and multiple aphthous stomatitis, bronchial asthma, an emphysematous lung, a ventricular septal defect and a bilateral inguinal hernia due to hyperextensibility and joint hypermobility. The other was a 17-year-old girl with the same syndrome and an atrial septal defect, a ventricular septal defect and patent ductus arteriosus. The combination of Ehlers-Danlos syndrome and congenital heart anomalies in these siblings suggest a common genetic defect to be the cause of these diseases.<br>(Internal Medicine 35: 200-202, 1996)

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  • Internal Medicine

    Internal Medicine 35 (3), 200-202, 1996

    一般社団法人 日本内科学会

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