Primrose syndrome
From Wikidoc - Reading time: 1 min
Primrose syndrome is a rare variably expressed genetic disorder characterised by (amongst other symptoms) ossification of the external ears and learning difficulties.
Identified first at the Royal National Larbert Institution in Scotland. Template:Disease-stub
Licensed under CC BY-SA 3.0 | Source: https://www.wikidoc.org/index.php/Primrose_syndrome8 views | ↧ Download this article as ZWI file
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