X-linked intellectual disability-retinitis pigmentosa syndrome

X-linked intellectual disability-retinitis pigmentosa syndrome is characterized by moderate intellectual deficit and severe, early-onset retinitis pigmentosa. It has been described in five males spanning three generations of one family. Some patients also had microcephaly. It is transmitted as an X-linked recessive trait.

Also known as: Aldred syndrome, chromosome xp11.3 deletion syndrome, X-linked recessive, retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion, retinitis pigmentosa and intellectual disability due to del(X)(p11.3), retinitis pigmentosa and intellectual disability due to monosomy Xp11.3, X-linked mental handicap-retinitis pigmentosa syndrome, chromosome Xp11.3 deletion syndrome, intellectual disability, X-linked, with retinitis pigmentosa

5 clinical trials for this condition and its sub-types, 0 tagged with X-linked intellectual disability-retinitis pigmentosa syndrome itself.