Unexpected findings in cervical spine in spondylometaphyseal dysplasia Sutcliff type FN1‐related

Author:

Ramos‐Mejía Rosario1ORCID,Heath Karen E.2345ORCID,Modamio‐Høybjør Silvia234ORCID,Huckstadt Victoria6ORCID,Calcagni Julián7ORCID,Remondino Rodrigo7ORCID,Fano Virginia1ORCID

Affiliation:

1. Growth and Development Department Hospital Garrahan Buenos Aires Argentina

2. Institute of Medical & Molecular Genetics (INGEMM), IdiPAZ, Hospital Universitario la Paz, UAM Madrid Spain

3. Skeletal Dysplasia Multidisciplinary Unit (UMDE‐ERN BOND), Hospital Universitario la Paz Madrid Spain

4. European Research Network on Rare BONe Disorders (ERN‐BOND) Madrid Spain

5. CIBERER, ISCIII Madrid Spain

6. Genetics Department Hospital Garrahan Buenos Aires Argentina

7. Spinal Pathology Department Hospital Garrahan Buenos Aires Argentina

Abstract

AbstractThe 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.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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