scholarly journals DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III

2009 ◽  
Vol 84 (5) ◽  
pp. 706-711 ◽  
Author(s):  
Nathalie Dagoneau ◽  
Marie Goulet ◽  
David Geneviève ◽  
Yves Sznajer ◽  
Jelena Martinovic ◽  
...  
2015 ◽  
Vol 55 (3) ◽  
pp. 155-157 ◽  
Author(s):  
Toshio Okamoto ◽  
Ken Nagaya ◽  
Yumi Kawata ◽  
Hiroko Asai ◽  
Etsushi Tsuchida ◽  
...  

2002 ◽  
Vol 5 (1) ◽  
pp. 91-96 ◽  
Author(s):  
Alessandro Corsi ◽  
Mara Riminucci ◽  
Mario Roggini ◽  
Paolo Bianco

A morphological study of the skeletal system in a case of short rib polydactyly syndrome type III (SRPS-III) documented a “bajonet” deformity of the ribs for misalignment and overlap of cartilaginous and bony ends. This deformity resulted from a ‘tandem’ change in endochondral bone formation that is, arrested orthotopic cartilage maturation and etherotopic perichondral cartilage differention and ossification. At the cartilaginous end, cartilage maturation and vascular invasion were absent. At the bony end, longitudinal bone growth occurred by a perichondral ectopic growth plate. ‘Miniature’ versions of this ‘tandem’ change were also demonstrated in the long bones of the limbs and included focally arrested orthotopic cartilage maturation at the growth plates, perichondral cartilage differentiation, and ossification within cartilage canals. Our morphological study indicates that a generalized loss of syncrony in cartilage removal and osteogenic differentiation occurs in all growth plates, albeit with varied expressivity, and represents, at tissue level, the mechanism by which the SRPS-III skeletal phenotype develops.


Sign in / Sign up

Export Citation Format

Share Document