Ehlers-Danlos Syndrome and Congenital Heart Anomalies

Toyoki Maeda, Yasuyo Suzuki, Shigehiko Haeno, Midori Asada, Ryouji Hiramatsu, Fumiaki Tanaka, Masaji Okada, Tomokazu Suzuki

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)200-202
Number of pages3
JournalInternal Medicine
Volume35
Issue number3
DOIs
Publication statusPublished - Mar 1996

All Science Journal Classification (ASJC) codes

  • Internal Medicine

Fingerprint Dive into the research topics of 'Ehlers-Danlos Syndrome and Congenital Heart Anomalies'. Together they form a unique fingerprint.

Cite this