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Up to: X-linked syndromic intellectual disability · Partial monosomy of the short arm of chromosome X
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.
This condition has no sub-types.