Ehlers danlos syndrome eds is characterized by a genetic defect that leads to production of abnormal collagen, resulting in modification of synthesis and structure of connective tissue. The ehlers danlos syndrome, a disorder with many faces. Ehlers danlos syndromes eds are a group of genetic connective tissue disorders. Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. Las articulaciones con tejidos conjuntivos debiles son mas propensas a dislocarse. Sed clasico ceds, sed similar al clasico classicallike eds, cleds, cardiacovalvular. Oral and craniofacial characteristics of a patient with ehlers danlos syndrome. Ehlers danlos types, the classic ehlers danlos can present with marfanoid habitus and or dysautonomia.
It has dominant autosomic inheritance and the genetic alteration is known col5a1 or col5a2. Case report ehlers danlos syndrome comprises a heterogeneous group of genetic disorders. These can be noticed at birth or in early childhood. No discrimina entre hombres y mujeres, ni entre razas o etnias claramente. Ehlers danlos syndromeeds hereditary connective tissue disorder autosomal dominant or recessive traits prevalence. It also can have osteopenia or osteoporosis, hernias, varicose veins, hemorrhoids and prolapse.
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