A dominantly inherited spondylometaphyseal dysplasia with "corner fractures" and congenital scoliosis
- PMID: 15666313
- DOI: 10.1002/ajmg.a.30567
A dominantly inherited spondylometaphyseal dysplasia with "corner fractures" and congenital scoliosis
Abstract
Spondylometaphyseal dysplasia (SMD) is a term applied to a varied group of skeletal dysplasias that principally involve the spine and the metaphyses of long bones. SMD Sutcliffe or "Corner Fracture" type is characterized by short stature, developmental coxa vara, fragmented appearance of the metaphyses ("corner fractures"), abnormally shaped vertebrae, odontoid hypoplasia, and dominant inheritance. We report a family with a dominantly inherited SMD with "corner fractures" and severe, congenital scoliosis but neither coxa vara nor odontoid abnormalities. This could either represent phenotypic variability in SMD-"Corner Fracture" type, or be a new, dominantly inherited SMD. The presence of severe, congenital scoliosis and short stature is present in all members of this family, and not typically seen in SMD-"Corner Fracture" type, supporting our hypothesis that this might represent a new, dominantly inherited SMD.
(c) 2005 Wiley-Liss, Inc.
Similar articles
-
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures".Am J Hum Genet. 2017 Nov 2;101(5):815-823. doi: 10.1016/j.ajhg.2017.09.019. Am J Hum Genet. 2017. PMID: 29100092 Free PMC article.
-
Developmental coxa vara associated with spondylometaphyseal dysplasia (DCV/SMD): "SMD-corner fracture type" (DCV/SMD-CF) demonstrated in most reported cases.Pediatr Radiol. 2000 Jan;30(1):14-24. doi: 10.1007/s002470050005. Pediatr Radiol. 2000. PMID: 10663502 Review.
-
Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.Am J Med Genet A. 2017 Mar;173(3):733-739. doi: 10.1002/ajmg.a.38059. Epub 2016 Nov 26. Am J Med Genet A. 2017. PMID: 27888646 Free PMC article.
-
Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures".Bone. 2019 Apr;121:163-171. doi: 10.1016/j.bone.2018.12.020. Epub 2018 Dec 30. Bone. 2019. PMID: 30599297
-
Spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type: report of a new patient and review of the literature.Am J Med Genet A. 2003 Oct 15;122A(3):252-6. doi: 10.1002/ajmg.a.20262. Am J Med Genet A. 2003. PMID: 12966527 Review.
Cited by
-
Molecular landscape of congenital vertebral malformations: recent discoveries and future directions.Orphanet J Rare Dis. 2024 Jan 30;19(1):32. doi: 10.1186/s13023-024-03040-0. Orphanet J Rare Dis. 2024. PMID: 38291488 Free PMC article. Review.
-
Hand Radiographs in Skeletal Dysplasia: A Pictorial Review.Indian J Radiol Imaging. 2023 Dec 15;34(2):291-308. doi: 10.1055/s-0043-1777320. eCollection 2024 Apr. Indian J Radiol Imaging. 2023. PMID: 38549896 Free PMC article. Review.
-
Spondylometaphyseal Dysplasia Corner Fracture (Sutcliffe) Type.Indian J Pediatr. 2016 Oct;83(10):1191-4. doi: 10.1007/s12098-016-2121-3. Epub 2016 Apr 30. Indian J Pediatr. 2016. PMID: 27130511
-
Comparative genomics uncovers the evolutionary history, demography, and molecular adaptations of South American canids.Proc Natl Acad Sci U S A. 2022 Aug 23;119(34):e2205986119. doi: 10.1073/pnas.2205986119. Epub 2022 Aug 15. Proc Natl Acad Sci U S A. 2022. PMID: 35969758 Free PMC article.
-
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures".Am J Hum Genet. 2017 Nov 2;101(5):815-823. doi: 10.1016/j.ajhg.2017.09.019. Am J Hum Genet. 2017. PMID: 29100092 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical