Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Two cases of the Prader-Willi syndrome with 46, XY/47, XY, + mar are reported. The majority of Prader-Willi patients with chromosome abnormalities have either 15/15 translocations or mosaicism. Both of these aberrations presumably occur after fertilization. A possible relationship between high parental age and chromosome abnormalities in the Prader-Willi syndrome is discussed.

OriginalsprogEngelsk
TidsskriftClinical Genetics
Vol/bind16
Udgave nummer3
Sider (fra-til)147-150
Antal sider4
ISSN0009-9163
DOI
StatusUdgivet - 1979

ID: 258037437