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Rev. méd. Chile ; 146(8): 938-942, ago. 2018. tab, graf
Artículo en Español | LILACS | ID: biblio-978779

RESUMEN

Ehlers Danlos Syndrome comprises a heterogeneous group of genetic disorders of the connective tissue, due to defects in collagen or its modifying enzymes. We report a 21 years old male presenting with translucent skin revealing the subcutaneous venous pattern. He had a thin face, large-appearing eyes, thin lips, thin nose, joint hypermotility and history of hip dysplasia. A vascular Ehlers Danlos Syndrome was suspected. However, the genetic study to confirm the diagnosis was not done.


Asunto(s)
Humanos , Masculino , Adulto , Adulto Joven , Síndrome de Ehlers-Danlos/diagnóstico , Heterogeneidad Genética , Enfermedades del Tejido Conjuntivo/genética , Enfermedades del Tejido Conjuntivo/diagnóstico por imagen , Técnicas de Diagnóstico Molecular , Síndrome de Ehlers-Danlos/genética
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