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Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.
Machol, Keren; Jain, Mahim; Almannai, Mohammed; Orand, Thibault; Lu, James T; Tran, Alyssa; Chen, Yuqing; Schlesinger, Alan; Gibbs, Richard; Bonafe, Luisa; Campos-Xavier, Ana Belinda; Unger, Sheila; Superti-Furga, Andrea; Lee, Brendan H; Campeau, Philippe M; Burrage, Lindsay C.
Afiliação
  • Machol K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Jain M; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Almannai M; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Orand T; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Lu JT; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Tran A; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Chen Y; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Schlesinger A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Gibbs R; Department of Pediatric Radiology, Texas Children's Hospital, Houston, Texas.
  • Bonafe L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Campos-Xavier AB; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Unger S; Centre for Molecular Diseases and Department of Pediatrics, Lausanne University Hospital (CHUV), University of Lausanne, Lausanne, Switzerland.
  • Superti-Furga A; Centre for Molecular Diseases and Department of Pediatrics, Lausanne University Hospital (CHUV), University of Lausanne, Lausanne, Switzerland.
  • Lee BH; Service of Medical Genetics, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
  • Campeau PM; Service of Medical Genetics, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
  • Burrage LC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
Am J Med Genet A ; 173(3): 733-739, 2017 Mar.
Article em En | MEDLINE | ID: mdl-27888646
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Fenótipo / Fraturas da Tíbia / Colágeno Tipo II / Estudos de Associação Genética / Transtornos do Crescimento / Articulação do Quadril Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child, preschool / Humans / Infant / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Fenótipo / Fraturas da Tíbia / Colágeno Tipo II / Estudos de Associação Genética / Transtornos do Crescimento / Articulação do Quadril Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child, preschool / Humans / Infant / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article