EHLERS-DANLOS SYNDROME - CLINICAL CASE-RE PORT PROBABLY OF TYPE-VIII

Authors
LANZI G OTTOLINI A VALENTI A BERARDINELLI A FRATICELLI D DYNE KM CETTA G
Citation
G. Lanzi et al., EHLERS-DANLOS SYNDROME - CLINICAL CASE-RE PORT PROBABLY OF TYPE-VIII, Rivista italiana di pediatria, 20(2), 1994, pp. 164-167
Citations number
NO
Categorie Soggetti
Pediatrics
Journal title
Rivista italiana di pediatria → ACNP
ISSN journal
03925161
Volume
20
Issue
2
Year of publication
1994
Pages
164 - 167
Database
ISI
SICI code
0392-5161(1994)20:2<164:ES-CCP>2.0.ZU;2-J
Abstract
The Ehlers-Danlos syndrome comprises a clinically, genetically and bio chemically heterogeneous group of connettive tissue disorders, current ly classified into nine types based on clinical manifestations and inh eritance pattern. The Authors describe a patient with sign of EDS and periodontitis and a three generation family hystory of premature teeth loss. Clinical findings are compared with other data available in the literature.