DOWN'S SYNDROME WITH X0/XY MOSAICISM
- 1 May 1976
- journal article
- research article
- Published by Wiley in Acta Paediatrica
- Vol. 65 (3) , 391-395
- https://doi.org/10.1111/j.1651-2227.1976.tb04903.x
Abstract
A 5 mo. old Chinese infant with combined Down''s syndrome and X0/XY mosaicism is presented. The phenotypical features of mongolism are classical and unmodified. The somatic effects of X0/XY mosaicism is that of incomplete masculinization with short phallus, hypospadias, bifid scrotum, urogenital sinus, and bilateral extra-abdominal infantile testicles. These features together with the absence of internal female organs and signs of Turner''s syndrome in this patient are different from the previous reported cases of mixed gonadal dysgenesis.Keywords
This publication has 15 references indexed in Scilit:
- Patient with Down's syndrome and male pseudohermaphroditism with a 47, XY, +21/46, X, +21 karyotypeClinical Genetics, 1974
- Trisomy 18 and 21 in two siblingsClinical Genetics, 1973
- A case of XYY Down's syndrome confirmed by autoradiography.Journal of Medical Genetics, 1971
- 21 trisomy with an XYY sex chromosome complementThe Journal of Pediatrics, 1966
- 21-TRISOMY AND XYYThe Lancet, 1965
- XXX 21-TRISOMYThe Lancet, 1964
- XO/XX MOSAICISM AND MONGOLISM IN THE SAME PERSONThe Lancet, 1964
- XXX 21-TRISOMY AND RETINOBLASTOMAThe Lancet, 1963
- The Klinefelter-mongolism type of double aneuploidyAnnals of Human Genetics, 1959
- THE CHROMOSOMES IN A PATIENT SHOWING BOTH MONGOLISM AND THE KLINEFELTER SYNDROMEThe Lancet, 1959