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Rev. bras. ortop ; 38(6): 357-361, jun. 2003. ilus
Artículo en Portugués | LILACS | ID: lil-360798

RESUMEN

The authors report two patients with chondroectodermal dysplasia, also called Ellis-van Creveld Syndrome. This rare, inherited disease of autossomal-recessive trait was diagnosed in two brothers. Both presented clinically with dwarfism, postaxial hand polydactyly, fingernail dysplasia, shortened limbs, heart and teeth problems, and other associated deformities. One of the children evolved to death from cardiac arrest, and the other is sound at 5 years of age. The main purpose of the orthopedic approach in this syndrome is to improve the function and appearance of affected hands.


Asunto(s)
Humanos , Masculino , Femenino , Recién Nacido , Preescolar , Síndrome de Ellis-Van Creveld
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