47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome

J P Fryns; A Kleczkowska; H Van den Berghe

47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome

Ann Genet. 1986;29(2):112-3.

Authors

J P Fryns, A Kleczkowska, H Van den Berghe

PMID: 3490205

Abstract

The present report summarizes the follow-up data from birth up to the age of 14 years in a male patient with Beckwith-Wiedemann syndrome and 47,XXY karyotype.

Publication types

Case Reports

MeSH terms

Beckwith-Wiedemann Syndrome / genetics*
Follow-Up Studies
Humans
Infant, Newborn
Karyotyping
Lymphocytes / cytology
Male
Sex Chromosome Aberrations*