Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.

@article{Clemens1996PittRogersDanksST,
  title={Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.},
  author={Michele Clemens and John T. Martsolf and John G. Rogers and Patricia A. Mowery-Rushton and Urvashi Surti and Elizabeth McPherson},
  journal={American journal of medical genetics},
  year={1996},
  volume={66 1},
  pages={
          95-100
        }
}
Pitt-Rogers-Danks syndrome (PRDS) is a rare, presumed autosomal recessive, syndrome with pre- and postnatal growth retardation, microcephaly, characteristic facial appearance, seizures, unusual palmar creases and developmental delay. Since the first description in 1984, only 7 cases have been reported. We report the identification of a 4p microdeletion in 2 new patients, who were previously diagnosed with PRDS, as well as the sibs in Pitt et al. [1984]. PRDS can no longer be considered… CONTINUE READING

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