MORM syndrome

MORM syndrome is characterized by the association of intellectual deficit, truncal obesity, retinal dystrophy and micropenis. It has been described in 14 individuals from a consanguineous family. It is transmitted in an autosomal recessive manner. The causative locus has been mapped to chromosome region 9q34.

Also known as: MORM syndrome, intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome, mental retardation, truncal obesity, retinal dystrophy, and micropenis, mental retardation-truncal obesity-retinal dystrophy-micropenis syndrome, MORMS, intellectual disability, truncal obesity, retinal dystrophy and micropenis, intellectual disability, truncal obesity, retinal dystrophy, and micropenis syndrome, mental retardation, truncal obesity, retinal dystrophy and micropenis

0 clinical trials for this condition and its sub-types, 0 tagged with MORM syndrome itself.