Wolfram-like syndrome – another face of a rare disease in children
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DOI: 10.1515/jpem-2021-0348
Abstract: Abstract Objectives The presence of two pathogenic variants in the WFS1 gene leads to the occurrence of a rare genetic disease in children – Wolfram syndrome (WFS), which includes insulin-dependent diabetes mellitus (DM), optic atrophy… read more here.
Keywords: children wolfram; wfs1 gene; like syndrome; disease children ... See more keywords