Abstract

CALLEA, Michele et al. Clinical and molecular study in a family with cleidocranial dysplasia. Arch. argent. pediatr. [online]. 2017, vol.115, n.6, pp.e440-e444. ISSN 0325-0075.  http://dx.doi.org/10.5546/aap.2017.e440.

Cleidocranial dysplasia is an uncommon bone dysplasia with an autosomal dominant inheritance pattern characterized by short stature, large fontanels, midface hypoplasia, absence or hypoplasia of clavicles and orodental alterations. This is produced by mutations in the RUNX2 gene located at 6p21.1. We report two male adolescents (cousins), with cleidocranial dysplasia who presented a heterozygous missense mutation (c.674G> A, p.R225Q) in the RUNX2 gene, characterized by severe phenotype, such as absent clavicles, but with variation in the delayed fontanel closure, dental abnormalities (anomalies in shape and number) and scoliosis, thus demonstrating intrafamilial variation in these patients with the same genotype.

Keywords : Cleidocranial dysplasia; RUNX2; c.674G>A; p.R225Q.

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