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Atelosteogenesis type III: orthopedic management.
- 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.
- Subjects :
- Abnormalities, Multiple diagnostic imaging
Abnormalities, Multiple genetics
Child, Preschool
Female
Filamins genetics
Hand Joints diagnostic imaging
Hand Joints surgery
Humans
Knee Joint diagnostic imaging
Knee Joint surgery
Mutation
Osteochondrodysplasias diagnostic imaging
Osteochondrodysplasias genetics
Radiography
Scoliosis diagnosis
Scoliosis surgery
Treatment Outcome
Ultrasonography, Prenatal
Abnormalities, Multiple surgery
Gait
Osteochondrodysplasias surgery
Subjects
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