scholarly journals Diastrophic Dysplasia, a Rare Cause of Congenital Dwarfism

2016 ◽  
Vol 1 (1) ◽  
Author(s):  
Srikanth Sankar Ravisankar
1999 ◽  
Vol 56 (1) ◽  
pp. 71-76 ◽  
Author(s):  
André Mégarbané ◽  
Fady A. Haddad ◽  
Soha Haddad-Zebouni ◽  
Mitri Achram ◽  
Georg Eich ◽  
...  

2006 ◽  
Vol 99 (11) ◽  
pp. 584-585
Author(s):  
M. Ramachandran ◽  
J. K Aronson

2002 ◽  
Vol 32 (9) ◽  
pp. 621-628 ◽  
Author(s):  
Ville M. Remes ◽  
Eino J. Marttinen ◽  
Mikko S. Poussa ◽  
Ilkka J. Helenius ◽  
Jari I. Peltonen

2011 ◽  
Vol 75 (5) ◽  
pp. 713-715 ◽  
Author(s):  
Sharon L. Cushing ◽  
Rebecca L. Swanson ◽  
Kathleen C.Y. Sie

2003 ◽  
Vol 85 (3) ◽  
pp. 441-447 ◽  
Author(s):  
ILKKA HELENIUS ◽  
VILLE REMES ◽  
KAJ TALLROTH ◽  
JARI PELTONEN ◽  
MIKKO POUSSA ◽  
...  

2018 ◽  
pp. 245-306
Author(s):  
Jürgen W. Spranger ◽  
Paula W. Brill ◽  
Christine Hall ◽  
Gen Nishimura ◽  
Andrea Superti-Furga ◽  
...  

This chapter further discusses bone dysplasias and includes discussion on achondrogenesis (type IB), atelosteogenesis type 2, diastrophic dysplasia, multiple epiphyseal dysplasia (recessive type [rMED]), Desbuquois dysplasia, chondrodysplasia with joint dislocations (IMPAD1/gPAPP type), Catel-Manzke syndrome, chondrodysplasia with congenital joint dislocations (CHST3-type), temtamy preaxial brachydactyly syndrome (TPBS), B4GALT7 deficiency, B3GAT3 deficiency, XYLT1 deficiency, spondyloepimetaphyseal dysplasia with joint laxity Beighton type, spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type), pseudodiastrophic dysplasia, and Steel syndrome. Each discussion includes major radiographic features, major clinical findings, genetics, major differential diagnoses, and a bibliography.


2016 ◽  
Vol 39 (1) ◽  
pp. 46-49
Author(s):  
Nasir Uddin Mahmud ◽  
Jagadish C Das ◽  
Mayen Uddin Mahmud ◽  
Mohammad Shamim Hasan ◽  
Rifat Taher ◽  
...  

Abstract not availableBangladesh J Child Health 2015; VOL 39 (1) :46-49


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