Sindrome de Langer Giedion: En Ingles

http://www.healthonnet.org/HONselect/RareDiseases/SP/C05.116.099.708.582.html
Síndrome de Langer-Giedion
Definición: Autosomal dominant disorder characterized by cone-shaped epiphyses in the hands and multiple cartilaginous exostoses.
Mental retardation and abnormalities of chromosome 8 are often present.
The exostoses in this syndrome appear identical to those of hereditary multiple exostoses (EXOSTOSES, HEREDITARY MULTIPLE).

Sinónimos:
Acrodisplasia V
Síndrome Tricorrinofalangiano Tipo II
Síndrome de Giedion-Langer
Vea relacionado:
Exostosis Múltiple Hereditaria

www.childsdoc.org The Child's Doctor [Children's Memorial Hospital, Chicago]
Brachydactyly in an affected adult woman and her three-year-old child; note widening of the proximal interphalangeal joints.
Copyright © JOEL M. CHARROW, MD

wimp.nsm.uh.edu
Copyright © The University of Houston Langer Giedion Syndrome Home Page
This is a G-banded ideogram of human chromosome 8. It shows the general location of LGS in relationship to the entire chromosome