Radiologic Features of Type II and Type XI Collagenopathies.

Abstract

Type II collagen is a major component of the cartilage matrix. Pathogenic variants (ie, disease-causing aberrations) in the type II collagen gene (COL2A1) lead to an abnormal structure of type II collagen, causing a large group of skeletal dysplasias termed type II collagenopathies. Because type II collagen is also located in the vitreous body of the eyes and inner ears, type II collagenopathies are commonly associated with vitreoretinal degeneration and hearing impairment. Type II collagenopathies can be radiologically divided into two major groups: the spondyloepiphyseal dysplasia congenita (SEDC) group and the Kniest-Stickler group. The SEDC group is characterized by delayed ossification of the juxtatruncal bones, including pear-shaped vertebrae. These collagenopathies comprise achondrogenesis type 2, hypochondrogenesis, SEDC, and other uncommon subtypes. The Kniest-Stickler group is characterized by disordered tubular bone growth that leads to "dumbbell" deformities. It comprises Kniest dysplasia and Stickler dysplasia type 1, whose radiographic manifestations overlap with those of type XI collagenopathies (a group of disorders due to abnormal type XI collagen) such as Stickler dysplasia types 2 and 3. This phenotypic overlap is caused by type II and type XI collagen molecules sharing part of the same connective tissues. The authors describe the diagnostic pathways to type II and type XI collagenopathies and the associated differential diagnoses. In addition, they review the clinical features and genetic bases of these conditions, which radiologists should know to participate in multidisciplinary care and translational research. Online supplemental material is available for this article. ©RSNA, 2020.

• Authors: Atsuhiko Handa, Giedre Grigelioniene, Gen Nishimura
• Journal: Radiographics : a review publication of the Radiological Society of North America, Inc (Radiographics) 2021 Jan-Feb Vol. 41 Issue 1 Pg. 192-209 ISSN: 1527-1323 [Electronic] United States
• PMID: 33186059 (Publication Type: Journal Article)

Topics

• Achondroplasia
• Cartilage
• Collagen Diseases (diagnostic imaging)
• Humans
• Hyaline Membrane Disease
• Infant, Newborn
• Osteochondrodysplasias (diagnostic imaging)