Home - Genetic Disorders of the Skeleton
The 13th Annual Skeletal Dysplasia Course will be held in Lausanne form July 1 to July 5, 2019.
The 2018 course will be held in Lausanne from July 9 to July 13.
Individuals with short stature and deformity have always been part of mankind.
The 11th Introductory Course on Skeletal Dysplasia was held at the Hotel Aquatis in Lausanne on July 3 to 7, 2017.
Applications are open for the 11th Course in the Diagnostic Approach to Skeletal Dysplasias that will be held in Lausanne from July 3 to July 7, 2017
Skeletal dysplasia, severe immune deficiency (presenting in the newborn as Omenn syndrome), and developmental delay: this newly recognized condition is caused by mutations in EXTL3, an enzyme responsible for the synthesis of heparan sulfate.
The 10th Skeletal Dysplasia Course was successfully completed.
Genetic ablation of the soluble frizzled-related protein 4, sFRP4, is the genetic basis of Pyle disease.
10th Skeletal Dysplasia Course 2016
Lausanne, July 4-8 2016
The 2015 Course has been completed successfully !
The 2014 Course has been completed successfully!
The 2013 Skeletal Dysplasia Course has been held in Lausanne
from July 1 to July 5, 2013