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Título : HLA COMPLEX IN WERNER'S DISEASE
Autor : Perez-Rojas, G.
Marcano, N.
Gonzalez, L.
Penchaszadeh, G.
Moya, P.
Bianco Colmenares, Nicolás E.
Abadi, I.
Palabras clave : Werner's Syndrome
recessive pattern
inheritance
consanguinity
family
individuals
Fecha de publicación : 23-Nov-1979
Editorial : Clinical Immunology National Center and National Center for Rheumatic Diseases, SAS-UCV.
Resumen : During the 8th International Workshop, we studied family 01, where five patients with Werner's disease were identified in the first generation. Werner's Syndrome is a rare entity with a recessive pattern of inheritance where consanguinity between parents is expected to be increased . In our family we found that individuals 300 and 301 were first cousins It is relevant at this point to rep ort that this family comes from Quibor, a small town in Venezuela, where a group of German immigrants sett led in the middle of t he 19th century, creating a highly inbred population. Quibor still maintains some German characteristics in architecture, habits, and people with Caucasian features.
URI : http://hdl.handle.net/123456789/13906
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