A Case of Ehlers-Danlos Syndrome
Ehlers-Danlos syndrome, an inherited connective tissue disorder, is characterized by skin hyperextensibility, joint hypermobility and skin fragility. The disease is at least classified into 10 types, I to X, based on clinical features, biochemical abnormalities of the connective tissue and the mode...
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Veröffentlicht in: | Shoni shikagaku zasshi = the Japanese journal of pedodontics 1989/03/25, Vol.27(1), pp.208-219 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | jpn |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Ehlers-Danlos syndrome, an inherited connective tissue disorder, is characterized by skin hyperextensibility, joint hypermobility and skin fragility. The disease is at least classified into 10 types, I to X, based on clinical features, biochemical abnormalities of the connective tissue and the mode of inheritance. A case is reported of a 6-year,8-month-old girl who showed the features of the Ehlers-Danlos syndrome type VII. |
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ISSN: | 0583-1199 2186-5078 |
DOI: | 10.11411/jspd1963.27.1_208 |