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_syndrome6 views | Status: cached on October 17 2025 17:15:28↧ Download this article as ZWI file
EncycloReader
is supported by the 
KSF