Unexpected findings in cervical spine in spondylometaphyseal dysplasia Sutcliff type FN1-related.

Abstract

The autosomal dominant spondylometaphyseal dysplasia Sutcliff type or corner fracture type FN1-related is characterized by a combination of metaphyseal irregularities simulating fractures ("corner fractures"), developmental coxa vara, and vertebral changes. It is linked to heterozygous mutations in FN1 and COL2A1. Vertebral changes as delayed vertebral ossification, ovoid vertebral bodies, anterior vertebral wedging, and platyspondyly have been observed in this condition, while odontoid abnormalities have not been reported. We report an odontoid anomaly in a girl with SMD-CF FN1-related showing the heterozygous variant c.505T>A; p.(Cys169Ser), presenting at 11.9 years of age with acute quadriparesis. Images showed spinal cord compression and injury associated with os odontoideum and C1-C2 instability. She required decompression and instrumented occipitocervical stabilization, suffering from residual paraparesis. This paper describes the first case of SMD-CF FN1-related accompanied by odontoid anomalies.

• Authors: Rosario Ramos-Mejía, Karen E Heath, Silvia Modamio-Høybjør, Victoria Huckstadt, Julián Calcagni, Rodrigo Remondino, Virginia Fano
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) (Nov 08 2023) ISSN: 1552-4833 [Electronic] United States
• PMID: 37940834 (Publication Type: Case Reports)
• Copyright: © 2023 Wiley Periodicals LLC.