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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1989 Jul;26(7):434–438. doi: 10.1136/jmg.26.7.434

Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndrome.

A Smith 1, I S Fraser 1, R P Shearman 1, P Russell 1
PMCID: PMC1015646  PMID: 2746615

Abstract

We describe four females from three families with blepharophimosis, epicanthus inversus, and ptosis who were found to have premature ovarian failure. In two families the inheritance was autosomal dominant and in one it was a new mutation. Two females had, in addition, dysmorphic facial features which have been described in other cases. We suggest that the aetiology of the blepharophimosis ovarian failure syndrome is a contiguous gene syndrome.

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Selected References

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  1. Chen Y. T., Mattison D. R., Bercu B. B., Schulman J. D. Resistance of the male gonad to a high galactose diet. Pediatr Res. 1984 Apr;18(4):345–348. doi: 10.1203/00006450-198404000-00008. [DOI] [PubMed] [Google Scholar]
  2. Connor J. M. Prenatal diagnosis of the Turner syndrome: what to tell the parents. Br Med J (Clin Res Ed) 1986 Sep 20;293(6549):711–712. doi: 10.1136/bmj.293.6549.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cooper H. E., Spellacy W. N., Prem K. A., Cohen W. D. Hereditary factors in the Stein-Leventhal syndrome. Am J Obstet Gynecol. 1968 Feb 1;100(3):371–387. doi: 10.1016/s0002-9378(15)33704-2. [DOI] [PubMed] [Google Scholar]
  4. Francke U., Harper J. F., Darras B. T., Cowan J. M., McCabe E. R., Kohlschütter A., Seltzer W. K., Saito F., Goto J., Harpey J. P. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions. Am J Hum Genet. 1987 Mar;40(3):212–227. [PMC free article] [PubMed] [Google Scholar]
  5. Fraser I. S., Russell P., Greco S., Robertson D. M. Resistant ovary syndrome and premature ovarian failure in young women with galactosaemia. Clin Reprod Fertil. 1986 Apr;4(2):133–138. [PubMed] [Google Scholar]
  6. Fraser I. S., Shearman R. P., Smith A., Russell P. An association among blepharophimosis, resistant ovary syndrome, and true premature menopause. Fertil Steril. 1988 Nov;50(5):747–751. doi: 10.1016/s0015-0282(16)60309-6. [DOI] [PubMed] [Google Scholar]
  7. Greenberg F., Valdes C., Rosenblatt H. M., Kirkland J. L., Ledbetter D. H. Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome. J Pediatr. 1986 Sep;109(3):489–492. doi: 10.1016/s0022-3476(86)80124-x. [DOI] [PubMed] [Google Scholar]
  8. Harper P. S. Isolating the gene for Duchenne muscular dystrophy. Br Med J (Clin Res Ed) 1986 Sep 27;293(6550):773–774. doi: 10.1136/bmj.293.6550.773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jones C. A., Collin J. R. Blepharophimosis and its association with female infertility. Br J Ophthalmol. 1984 Aug;68(8):533–534. doi: 10.1136/bjo.68.8.533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kohn R., Romano P. E. Blepharoptosis, blepharophimosis, epicanthus inversus, and telecanthus--a syndrome with no name. Am J Ophthalmol. 1971 Sep;72(3):625–632. doi: 10.1016/0002-9394(71)90864-6. [DOI] [PubMed] [Google Scholar]
  11. Krauss C. M., Turksoy R. N., Atkins L., McLaughlin C., Brown L. G., Page D. C. Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome. N Engl J Med. 1987 Jul 16;317(3):125–131. doi: 10.1056/NEJM198707163170301. [DOI] [PubMed] [Google Scholar]
  12. Moore J. W., Hyman S., Antonarakis S. E., Mules E. H., Thomas G. H. Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)]. Hum Genet. 1986 Apr;72(4):297–302. doi: 10.1007/BF00290952. [DOI] [PubMed] [Google Scholar]
  13. Moraine C., Titeca C., Delplace M. P., Grenier B., Lenoel Y., Ribadeau-Dumas J. L. Blépharophimosis familial et stérilité féminine: pléiotropisme ou gènes liés. J Genet Hum. 1976 Nov;24 (Suppl):125–132. [PubMed] [Google Scholar]
  14. Ohdo S., Madokoro H., Sonoda T., Hayakawa K. Mental retardation associated with congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth. J Med Genet. 1986 Jun;23(3):242–244. doi: 10.1136/jmg.23.3.242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Oley C., Baraitser M. Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome) J Med Genet. 1988 Jan;25(1):47–51. doi: 10.1136/jmg.25.1.47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Say B., Barber N. Mental retardation with blepharophimosis. J Med Genet. 1987 Aug;24(8):511–511. doi: 10.1136/jmg.24.8.511-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Schmickel R. D. Contiguous gene syndromes: a component of recognizable syndromes. J Pediatr. 1986 Aug;109(2):231–241. doi: 10.1016/s0022-3476(86)80377-8. [DOI] [PubMed] [Google Scholar]
  18. Townes P. L., Muechler E. K. Blepharophimosis, ptosis, epicanthus inversus, and primary amenorrhea. A dominant trait. Arch Ophthalmol. 1979 Sep;97(9):1664–1666. doi: 10.1001/archopht.1979.01020020232010. [DOI] [PubMed] [Google Scholar]
  19. Yunis J. J. High resolution of human chromosomes. Science. 1976 Mar 26;191(4233):1268–1270. doi: 10.1126/science.1257746. [DOI] [PubMed] [Google Scholar]
  20. Zlotogora J., Sagi M., Cohen T. The blepharophimosis, ptosis, and epicanthus inversus syndrome: delineation of two types. Am J Hum Genet. 1983 Sep;35(5):1020–1027. [PMC free article] [PubMed] [Google Scholar]

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