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Rev. méd. Chile ; 146(8): 938-942, ago. 2018. tab, graf
Article in Spanish | LILACS | ID: biblio-978779

ABSTRACT

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.


Subject(s)
Humans , Male , Adult , Young Adult , Ehlers-Danlos Syndrome/diagnosis , Genetic Heterogeneity , Connective Tissue Diseases/genetics , Connective Tissue Diseases/diagnostic imaging , Molecular Diagnostic Techniques , Ehlers-Danlos Syndrome/genetics
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