Biopsy-proven multiple sclerosis in an adult patient with atypical craniometaphyseal dysplasia

Jacopo C. Di Francesco, Giuseppe Isimbaldi, Maria Francesca Bedeschi, Barbara Castellotti

Research output: Contribution to journalArticlepeer-review

Abstract

Craniometaphyseal dysplasia (CMD) is a rare condition characterised by progressive, diffuse hyperostosis of cranial and long bones, with compression of cranial nerves, linked to mutations in ANKH or GJA1 genes. Here we describe an adult case with clinical features of CMD, who developed cerebral expansive lesion of undetermined nature. Brain biopsy revealed active demyelinating lesions, consistent with multiple sclerosis. The genetic screening of target genes for CMD (ANKH and GJA1) resulted negative in this patient. The peculiar clinical association and the negativity of genetic analyses allow to hypothesise that other genetic causes, not already known, are responsible for the combination of these pathological conditions. Future studies aim to identify the genetic causes of CMD, which will be important to further understand the pathogenetic mechanism of this rare and invalidating disease.

Original languageEnglish
Article number223390
JournalBMJ Case Reports
Volume2018
DOIs
Publication statusPublished - Jan 1 2018

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'Biopsy-proven multiple sclerosis in an adult patient with atypical craniometaphyseal dysplasia'. Together they form a unique fingerprint.

Cite this