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
Hauptverfasser: Seki, Mitsuko, Iwasaki, Mitsuhide, Takei, Kenji, Maeda, Takahide
Format: Artikel
Sprache:jpn
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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.
ISSN:0583-1199
2186-5078
DOI:10.11411/jspd1963.27.1_208