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Prieto syndrome | RareConnect | RareConnect.io

/X-linked syndromic intellectual disability

/Prieto syndrome

Prieto syndrome

Rare Disease

MONDO:0010667

Also Known As

Prieto syndrome, X-linked recessivePrieto-Badia-Mulas syndromeX-linked intellectual disability-dysmorphism-cerebral atrophy syndromeMRXS2PRSPrieto X-linked intellectual disability syndromePrieto X-linked mental retardation syndromeintellectual disability, X-linked, syndromic 2intellectual disability, X-linked, with Dysmorphism and cerebral atrophymental retardation, X-linked, syndromic 2mental retardation, X-linked, with Dysmorphism and cerebral atrophy

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:309610 ↗

Orphanet

Orphanet:2958 ↗

GARD

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