Sospecha diagnóstica de síndrome de Ehlers Danlos tipo vascular: Reporte de un caso y revisión de literatura.
Palabras clave:
Connective Tissue Diseases, Ehlers-Danlos Syndrome, Genetic Diseases, InbornResumen
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.Descargas
Publicado
2018-07-25
Cómo citar
Cevallos B, C., Vargas, E., González B, S., & Molgó, M. (2018). Sospecha diagnóstica de síndrome de Ehlers Danlos tipo vascular: Reporte de un caso y revisión de literatura. Revista Médica De Chile, 146(8). Recuperado a partir de https://mail.revistamedicadechile.cl/index.php/rmedica/article/view/6324
Número
Sección
Reporte de Caso Clínico