Further expansion of the mutational spectrum of spondylo-meta-epiphyseal dysplasia with abnormal calcification View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-06-08

AUTHORS

Gizem Ürel-Demir, Pelin Ozlem Simsek-Kiper, Özlem Akgün-Doğan, Rahşan Göçmen, Zheng Wang, Naomichi Matsumoto, Noriko Miyake, Gülen Eda Utine, Gen Nishimura, Shiro Ikegawa, Koray Boduroglu

ABSTRACT

Spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, is a rare autosomal recessive disorder of the skeleton characterized by disproportionate short stature with narrow chest and dysmorphic facial features. The skeletal manifestations include platyspondyly, short flared ribs, short tubular bones with abnormal metaphyses and epiphyses, severe brachydactyly, and premature stippled calcifications in the cartilage. The abnormal calcifications are so distinctive as to point to the definitive diagnosis. However, they may be too subtle to attract diagnostic attention in infancy. Homozygous variants in DDR2 cause this disorder. We report on a 5-year-old girl with the classic phenotype of SMED, SL-AC in whom a novel homozygous nonsense mutation in DDR2 was detected using exome sequencing. More... »

PAGES

1003-1007

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s10038-018-0473-4

DOI

http://dx.doi.org/10.1038/s10038-018-0473-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1104454579

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29884795


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