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Atelosteogenesis type III: orthopedic management.

Authors :
Sarikaya IA
Gorgun B
Erdal OA
Source :
Journal of pediatric orthopedics. Part B [J Pediatr Orthop B] 2017 Nov; Vol. 26 (6), pp. 546-551.
Publication Year :
2017

Abstract

Atelosteogenesis type III is a rare autosomal dominant skeletal dysplasia caused by mutations in the synthesis of the protein filamin B (FLNB). The mutation in the gene coding for FLNB causes the osteochondrodysplastic features of this disorder. Clinically, osteochondrodysplasia causes unbalanced skeletal maturation and absent or mostly hypoplastic bones, such as the pelvis, vertebrae, ribs, or long bones. In the literature, an orthopedic management for this disorder has not been well described. We report the case and orthopedic management of a 6-year-old female patient with atelosteogenesis type III after 3 years of follow-up.

Details

Language :
English
ISSN :
1473-5865
Volume :
26
Issue :
6
Database :
MEDLINE
Journal :
Journal of pediatric orthopedics. Part B
Publication Type :
Academic Journal
Accession number :
27258362
Full Text :
https://doi.org/10.1097/BPB.0000000000000338