A CASE OF PRADER‐WILLI SYNDROME IN A GIRL WITH A SMALL EXTRA CHROMOSOME
- 1 March 1971
- journal article
- case report
- Published by Wiley in Acta Paediatrica
- Vol. 60 (2) , 222-226
- https://doi.org/10.1111/j.1651-2227.1971.tb06646.x
Abstract
Summary: A characteristic case of Prader‐Willi syndrome is reported in a girl who showed, additionally, the presence of a small extra chromosome, possibly a fragment of a D or G group chromosome. Available members of the proposita's family were found to be phenotypically and cytologically normal. The case is compared with those previously reported.Keywords
This publication has 3 references indexed in Scilit:
- HUMAN POPULATION CYTOGENETICSBritish Medical Bulletin, 1969
- Prader‐Willi Syndrome in Boy of Ten with PrediabetesActa Paediatrica, 1964
- Chromosomal Translocation in a Mentally Deficient Child with CryptorchidismActa Paediatrica, 1963