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Potocki-Shaffer syndrome
Genetics:
- associated with defects in EXT2 & ALX4
- contiguous gene syndrome due to proximal deletion of chromosome 11p11.2, including EXT2 & ALX4
Clinical manifestations:
- parietal foramina 2
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 601224
References
(OMIM :accession 601224