Title | Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies. |
Publication Type | Journal Article |
Year of Publication | 2017 |
Authors | Machol, K, Jain, M, Almannai, M, Orand, T, Lu, JT, Tran, A, Chen, Y, Schlesinger, A, Gibbs, RA, Bonafe, L, Campos-Xavier, ABelinda, Unger, S, Superti-Furga, A, Lee, BH, Campeau, PM, Burrage, LC |
Journal | Am J Med Genet A |
Volume | 173 |
Issue | 3 |
Pagination | 733-739 |
Date Published | 2017 Mar |
ISSN | 1552-4833 |
Keywords | Alleles, Amino Acid Substitution, Bone Diseases, Developmental, Child, Preschool, Collagen Type II, Diagnosis, Differential, Exome, Genetic Association Studies, Genotype, Growth Disorders, High-Throughput Nucleotide Sequencing, Hip Joint, Humans, Infant, Male, Mutation, Osteochondrodysplasias, Phenotype, Radiography, Tibial Fractures |
Abstract | Spondylometaphyseal dysplasia (SMD) corner fracture type (also known as SMD "Sutcliffe" type, MIM 184255) is a rare skeletal dysplasia that presents with mild to moderate short stature, developmental coxa vara, mild platyspondyly, corner fracture-like lesions, and metaphyseal abnormalities with sparing of the epiphyses. The molecular basis for this disorder has yet to be clarified. We describe two patients with SMD corner fracture type and heterozygous pathogenic variants in COL2A1. These two cases together with a third case of SMD corner fracture type with a heterozygous COL2A1 pathogenic variant previously described suggest that this disorder overlaps with type II collagenopathies. The finding of one of the pathogenic variants in a previously reported case of spondyloepimetaphyseal dysplasia (SEMD) Strudwick type and the significant clinical similarity suggest an overlap between SMD corner fracture and SEMD Strudwick types. © 2016 Wiley Periodicals, Inc. |
DOI | 10.1002/ajmg.a.38059 |
Alternate Journal | Am J Med Genet A |
PubMed ID | 27888646 |
PubMed Central ID | PMC5315610 |
Grant List | K08 DK106453 / DK / NIDDK NIH HHS / United States U54 HG006542 / HG / NHGRI NIH HHS / United States T32 GM007526 / GM / NIGMS NIH HHS / United States U54 HD083092 / HD / NICHD NIH HHS / United States U54 HG003273 / HG / NHGRI NIH HHS / United States P30 HD024064 / HD / NICHD NIH HHS / United States P01 HD070394 / HD / NICHD NIH HHS / United States |
Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.
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