Hyperphosphatasia with mental retardation syndrome is a heterogeneous genetic condition. Two siblings aged 5 years and 3 years were evaluated for global development delay and facial dysmorphism. A novel missense variant, c.851A>G (p.H284R, NM_033419.3), in was identified using whole-exome sequencing. Assays for elevated alkaline phosphatase and exome sequencing can be useful for the diagnosis of hyperphosphatasia with mental retardation syndrome.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548534 | PMC |
http://dx.doi.org/10.1055/s-0037-1599148 | DOI Listing |
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