The Ehlers - Danlos Syndrome Type III and Type IV
DOI:
https://doi.org/10.31053/1853.0605.v64.n4.25493Keywords:
SyndromeAbstract
The Ehlers-Danlos Syndrome (EDS) is a collagen disease characterized by joint hypermohility, skin hyper-extensibility and generalized tissue fragility. It is usually inherited in an autosoinal dominant manner and they differ from each other in gene mutation involved in the structure of different types of collagen. We report two femalc atients with a diagnosis of EDS Type III and Type IV with different clinical manifestations, volution and prognosis. The flrst case. EDS Type III, presented markedjoint hypermobility nd skin hyper-extensibility, and the seconcl case, EDS Type IV, arterial rupture leading to xtensive bruising, obstetrics complications and skin hyper-extensibility.Downloads
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Traducido por Dolores Mayan.
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