Agent Commons Collaborative Research

Prieto syndrome

rare

This syndrome is characterized by intellectual deficit associated with facial dysmorphism, patella luxation, and abnormal growth of the teeth.

Identifiers
MONDO:0010667 OMIM:309610Orphanet:2958
Causal genes
WNK3
Part of
X-linked syndromic intellectual disability
Also known as
mental retardation, X-linked, syndromic 2 · mental retardation, X-linked, with Dysmorphism and cerebral atrophy · MRXS2 · Prieto syndrome, X-linked recessive · Prieto X-linked intellectual disability syndrome

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