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Research Article

Regional variation in blindness in children due to microphthalmos, anophthalmos and coloboma

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Pages 127-138 | Published online: 08 Jul 2009

References

  • Foster A, Gilbert C. Epidemiology ofvisual impairment in children. In: Taylor D, editor. Paediatric Ophthalmology, 2nd Edition. Oxford: Blackwell Science Ltd., 1996:3–12.
  • Stoll C, Alembik Y, Dott B, Roth MP.Epidemiology of congenital eye malformations in 131,760 consecutive births. Ophthalm Paediat Genet 1992; 13: 179–86.
  • Warburg M. Classification of microphthalmos and coloboma. J Med Genet 1993;30:664–9.
  • Bermejo E, Martinez-Frias M-L. Congenital eye malformations: clinical-epidemiological analysis of 1,124,654 consecutive births in Spain. Am J Med Genet 1998;75:497–504.
  • Czeizel AE, Intody Z, Modell B. What proportion of congenital abnormalities can be prevented? Br Med J 1993;3o6: 499–503.
  • Clementi M, Tenconi R, Bianchi F, Botto L, Calabro A, Calzolari E, et al. Congenital eye malformations: a descriptive epidemiologic study in about one million newborns in Italy. Birth Defects 1996;30:413–24.
  • Kallen B, Robert E, Harris J. Thedescriptive epidemiology of anophthalmia and microphthalmia. Int J Epidemiol 1996;25:1009–16.
  • Metropolitan Atlanta Congenital Defects Program (MACDP) 1968-1991. Data for birth defects prevention. Teratology 1993;48:545-.709.
  • Dolk H, Busby A, Armstrong BG, Walls PH. Geographical variation in anophthalmia and microphthalmia in England, 1988-94. Br Med J 1998; 317:905–9.
  • Fraser GR, Friedman Al. The Causes of Blindness in Childhood. Baltimore: John Hopkins Press, 1967.
  • Fujiki K, Nakajima A, Yasuda N, Tanabe U, Kabasawa K. Genetic analysis of microphthalmos. Ophthalm Paediat Genet 1992; I :139–49.
  • International Council for the Education of the Visually Handicapped, Resource Directory. Bensheim, Germany, 1986.
  • Sil A. Childhood Blindness in West Bengal. Dissertation for Masters degree in Community Eye Health. ICEH, London, 1998.
  • Dandona L, Williams JD, Williams BC, Rao GN. Population-based assessment of childhood blindness in southern India. Arch Ophthalmol 1998;116:545–6.
  • Gilbert C, Foster A, Negrel AD, Thylefors B. Childhood blindness: a new form for recording causes of visual loss in children. Bull WHO 1993;71:485–9.
  • Eckstein MB, Foster A, Gilbert CE. Causes of childhood blindness in Sri Lanka: results from children attending six schools for the blind. Br J Ophthalmol 1995;79:633–6.
  • Foster A, Gilbert CE. Epidemiology of childhood blindness. Eye 1992;6:173–6.
  • Gilbert CE, Anderton L, Dandona L, Foster A. Prevalence of visual impairment in children: A review of available data. Ophthalm Epidemiol 1999;6:73–82.
  • Dandona L, Gilbert CE, Rahi JS, Rao GN. Planning to reduce childhood blindness in India. Ind J Ophthalmol 1998;46:117–22.
  • Warburg M. Small eyes: descriptional misconceptions [letter]. Am J Med Genet 1995;59:388–9.
  • Weiss AH, Kousseff BG, Ross EA, Longbottom J. Complex microphthalmos. Arch Ophthalmol 1989;107:1619–24.
  • Weiss AH, Kousseff BG, Ross EA, Longbottom J. Simple microphthal-mos. Arch Ophthalmol 1989;107: 1625–30.
  • Bateman JB. Microphthalmos. Int Ophthalmol Clin 1984;24:87–107.
  • Warburg M, Friedrich U. Coloboma and microphthalmos in chromosomal aberrations. Chromosomal aberrations and neural crest cell developmental field. Ophthalm Paediat Genet 1987;8: 105–18.
  • Warburg M. An update on microphthalmos and coloboma. A brief survey of genetic disorders with microphthalmos and coloboma. Ophthalm Paediat Genet 1998;12:57–63.
  • Pagon RA. Ocular coloboma. Surv Ophthalmol 1981;25:223–36.
  • Freund C, Horsford DJ, McInnes RR. Transcription factor genes and the developing eye: A genetic perspective. Human Molec Genet 1996;5:1471–88.
  • Sanyusin P, McNoe LA, Sullivan MJ, Weaver RG, Eccles MR. Mutation of PAX2 in two siblings with renal coloboma syndrome. Human Molec Genet 1995;4: 2183–4.
  • Bessant DAR, Khaliq S, Hameed A, Anwar K, Mehdi SQ, Payne AM, Bhattacharya SS. A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. Am J Hum Genet 1998;62: 1113–6.
  • Graham CA, Redmond RM, Nevin NC. X-linked clinical anophthalmos: localization of the gene to Xq27-Xq28. Ophthalm Paediat Genet 1991; 12:43–8.
  • Brunquell PJ, Papale JH, Horton JC. Sex-linked hereditary bilateral anophthalmos. Arch Ophthalmol 1984;102:108–13.
  • Bittles AH, Grant JC, Shami SA. Consanguinity as a determinant of reproductive behaviour and mortality in Pakistan. Int J Epidemiol 1993;22: 463–7.
  • Gilbert C, Rahi J, Eckstein M, Foster A. Hereditary disease as a cause of childhood blindness: regional variation. Ophthalm Genet 1995;16:1 - DD.
  • Cao A, Rosatelli MC, Galanello R. Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experience. Ciba Found Symp 1996; 197:137–51.
  • Smith RS, Roderick TH, Sundberg JP. Microphthalmia and associated abnormalities in inbred black mice. Lab Anim Sci 1994;44:551–60.
  • Hale F. The relation of vitamin A to anophthalmos in pigs. Am J Ophthalmol 1935;18:1087–93.
  • Morriss-Kay GM, Ward SJ. Retinoids and mammalian development. Int Rev Cytol 1999;188:73–131.
  • Lamba PA, Sood NN. Congenital microphthalmos and colobomata in maternal vitamin A deficiency. Ind J Paediat Ophthalmol 1968;5:115–7.
  • McLarren DS, Frigg M. Sight and Life Manual on Vitamin A deficiency disorders (VADD). First edition. Basel, Switzerland, 1997:96.
  • WHO Global Prevalence of Vitamin A Deficiency Monograph WHO/ NUT/95.3, 1995.
  • Rahi JS, Sripathi S, Gilbert CE, Foster A. Childhood blindness in India: causes in 1318 blind school students in nine states. Eye 1995;9: 545–50.
  • Rahi JS, Sripathi S, Gilbert CE, Foster A. The importance of prenatal factors in childhood blindness in India. Dev Med & Child Neurol 1997;39:449–55.
  • Milunsky A, Ulcickas M, Rothman KJ. Maternal heat exposure and neural tube defects. J Am Med Assoc 1992;268:882–5.
  • Walker B. The effect of maternal fever on fetal development. Birth Res News 1996;1:2–3.

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