Skip to main content
PMC home page
British Heart Journal logoLink to British Heart Journal
. 1972 Jan;34(1):41–46. doi: 10.1136/hrt.34.1.41

Congenital heart disease in male and female subjects with somatic features of Turner's syndrome and normal sex chromosomes (Ullrich's and related syndromes).

D C Siggers, P E Polani
PMCID: PMC487088  PMID: 4400623

Full text

PDF
45

Images in this article

43Image
on p.43

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CARON P., MIEHER W. C., MELLINGER R. C., GREEN E. W. TURNER'S SYNDROME IN MALES. Henry Ford Hosp Med Bull. 1964 Mar;12:121–133. [PubMed] [Google Scholar]
  2. CHU E. H., WARKANY J., ROSENSTEIN R. B. Chromosome complement in a case of the "male Turner syndrome". Lancet. 1961 Apr 15;1(7181):786–788. doi: 10.1016/s0140-6736(61)90116-7. [DOI] [PubMed] [Google Scholar]
  3. Chaves-Carballo E., Hayles A. B. Ullrich-Turner syndrome in the male: review of the literature and report of a case with lymphocytic (Hashimoto's) thyroiditis. Mayo Clin Proc. 1966 Dec;41(12):843–854. [PubMed] [Google Scholar]
  4. EMERIT I., DEGROUCHY J., CORONE P., VERNANT P., LAVAL-JEANTET M. AG'EN'ESIE SACROCOCCYGIENNE ET SYNDROME DE BONNEVIE-ULLRICH. ETUDE G'EN'ETIQUE ET CHROMOSOMIQUE. Acta Genet Med Gemellol (Roma) 1964 Jan;13:69–89. [PubMed] [Google Scholar]
  5. FUTTERWEIT W., CHAPMAN M. L., SALVANESCHI J. P., MOLOSHOK R. E. Multiple congenital defects in a twelve year old boy with cryptorchidism--"male Turner's syndrome". Metabolism. 1961 Dec;10:1074–1084. [PubMed] [Google Scholar]
  6. Ferrier P. E., Ferrier S. A. Turner's phenotype in the male. Pediatrics. 1967 Oct;40(4):575–585. [PubMed] [Google Scholar]
  7. GRUMBACH M. M., BARR M. L. Cytologic tests of chromosomal sex in relation to sexual anomalies in man. Recent Prog Horm Res. 1958;14:255–334. [PubMed] [Google Scholar]
  8. GUSTAVSON K. H., HAGBERG B., KNUTSON H., SJOELIN S. THE PTERYGIUM-COLLI SYNDROME IN THE MALE. A CLINICAL, HISTOLOGICAL, AND CYTOGENETIC STUDY OF TWO CASES. Acta Paediatr. 1964 Sep;53:454–464. doi: 10.1111/j.1651-2227.1964.tb07251.x. [DOI] [PubMed] [Google Scholar]
  9. HALONEN P. I., SEPPALA T., HAKKILA J. Turner's syndrome in a man. Acta Med Scand. 1956 Feb 29;153(6):427–432. doi: 10.1111/j.0954-6820.1955.tb18247.x. [DOI] [PubMed] [Google Scholar]
  10. Migeon B. R., Whitehouse D. Familial occurrence of the somatic phenotype of Turner's syndrome. Johns Hopkins Med J. 1967 Feb;120(2):78–80. [PubMed] [Google Scholar]
  11. Noonan J. A. Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease. Am J Dis Child. 1968 Oct;116(4):373–380. doi: 10.1001/archpedi.1968.02100020377005. [DOI] [PubMed] [Google Scholar]
  12. Nora J. J., Sinha A. K. Direct familial transmission of the Turner phenotype. Am J Dis Child. 1968 Oct;116(4):343–350. doi: 10.1001/archpedi.1968.02100020347001. [DOI] [PubMed] [Google Scholar]
  13. POLANI P. E. Turner's syndrome and allied conditions. Clinical features and chromosome abnormalities. Br Med Bull. 1961 Sep;17:200–205. doi: 10.1093/oxfordjournals.bmb.a069909. [DOI] [PubMed] [Google Scholar]
  14. Polani P. E. Chromosomal abnormalities and congenital heart disease. Guys Hosp Rep. 1968;117(4):323–337. [PubMed] [Google Scholar]
  15. Wright N. L., Summitt R. L., Ainger L. E. Noonan's syndrome and Ebstein's malformation of the tricuspid valve. Am J Dis Child. 1968 Oct;116(4):367–372. doi: 10.1001/archpedi.1968.02100020371004. [DOI] [PubMed] [Google Scholar]

Articles from British Heart Journal are provided here courtesy of BMJ Publishing Group

RESOURCES