| Literature DB >> 30359775 |
Noor Ul Ain1, Muddassar Iqbal2, Helena Valta3, Christopher A Emerling4, Sufian Ahmed2, Outi Makitie5, Sadaf Naz6.
Abstract
Acromesomelic dysplasia are a heterogeneous group of disorders with variable spectrum and severity of skeletal anomalies in the affected individuals. Acromesomelic dysplasia type Maroteaux (AMDM) is characterized by extreme shortening of the forelimbs and disproportionate short stature. Several homozygous inactivating mutations in NPR2 have been identified in different AMDM patients. We report five novel variants in affected individuals in four different families. These include two nonsense and three missense variants. This study broadens the genotypic spectrum of NPR2 mutations in individuals with AMDM and also describes the intra- and inter-familial phenotypic variability due to NPR2 variants.Entities:
Keywords: AMDM; Acromesomelic dysplasia; NPR2; Short stature; Skeletal dysplasia
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Year: 2018 PMID: 30359775 DOI: 10.1016/j.ejmg.2018.10.006
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708