Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia - PubMed (original) (raw)

. 2017 Mar;62(3):437-441.

doi: 10.1038/jhg.2016.136. Epub 2016 Nov 10.

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Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia

Long Guo et al. J Hum Genet. 2017 Mar.

Abstract

Osteosclerotic metaphyseal dysplasia (OSMD) is a rare skeletal dysplasia characterized by osteosclerotic metaphyses with osteopenic diaphyses of the long tubular bones. Our previous study identified a homozygous elongation mutation in leucine-rich repeat kinase 1 gene (LRRK1) in a patient with OSMD and showed that Lrrk1 knockout mice exhibited phenotypic similarity with OSMD. Here we report a second LRRK1 mutation in Indian sibs with OSMD. They had homozygous mutation (c.5971_5972insG) that produces an elongated mutant protein (p.A1991Gfs*31) similar to the first case. The sibs had normal stature, normal intelligence and recurrent fractures. The common radiographic feature was asymmetric and variable sclerosis of vertebral end plates, pelvic margin and metaphyses of tubular bones. One of the sibs had facial dysmorphisms, dentine abnormalities and acro-osteolysis. A comparison between the three OSMD cases with LRRK1 mutations with different ages suggested that the sclerotic lesions resolved with age. Our findings further support that LRRK1 would cause a subset of OSMD cases.

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References

    1. Clin Genet. 2015 Apr;87(4):395-7 - PubMed
    1. Genome Res. 2010 Sep;20(9):1297-303 - PubMed
    1. J Med Genet. 2016 Aug;53(8):568-74 - PubMed
    1. J Bone Miner Res. 2013 Sep;28(9):1962-74 - PubMed
    1. Mol Biol Evol. 2006 Dec;23 (12 ):2423-33 - PubMed

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