Trisomy 18 in Kuwait

International Journal of Epidemiology

Volumn 28, Issue 4, 1999, Pages 711-716

  Naguib, Kamal Kamel ^a   Al Awadi, S A ^a   Moussa, M A A ^a   Bastaki, L ^a   Gouda, S ^a   Redha, M A ^a   Mustafa, F ^a   Tayel, S M ^a   Abulhassan, S A ^a   Murthy, D S K ^a  

^a NONE

Author keywords

Kuwait; Maternal age; Trisomy 18

Indexed keywords

CHILD HEALTH; HEALTH RISK; RISK FACTOR;

ABORTION; ADULT; ARTICLE; BIRTH ORDER; CASE CONTROL STUDY; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; EDWARDS SYNDROME; FEMALE; GASTROINTESTINAL DISEASE; HUMAN; KUWAIT; MAJOR CLINICAL STUDY; MALE; MATERNAL AGE; NEWBORN; NEWBORN DEATH; PATERNAL AGE; PRIORITY JOURNAL; REGRESSION ANALYSIS; RISK FACTOR; SEASONAL VARIATION; SURVIVAL; TRISOMY 18;

AGE FACTORS; ARAB COUNTRIES; ASIA; CASE CONTROL STUDIES; CHROMOSOME ABNORMALITIES; DEMOGRAPHIC FACTORS; DEVELOPING COUNTRIES; DISEASES; INFANT; KUWAIT; MATERNAL AGE; NEONATAL DISEASES AND ABNORMALITIES; PARENTAL AGE; PATERNAL AGE; POPULATION; POPULATION CHARACTERISTICS; RESEARCH METHODOLOGY; RESEARCH REPORT; STUDIES; WESTERN ASIA; YOUTH;

ABNORMALITIES, MULTIPLE; ADULT; AGE DISTRIBUTION; BIRTH RATE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 18; CONSANGUINITY; FEMALE; HUMANS; INFANT, NEWBORN; KUWAIT; MALE; MATERNAL AGE; MIDDLE AGED; PATERNAL AGE; PREGNANCY; PREVALENCE; RETROSPECTIVE STUDIES; RISK FACTORS; SEX DISTRIBUTION; SURVIVAL RATE; TRISOMY;

KUWAIT;

EID: 0032771040     PISSN: 03005771     EISSN: None     Source Type: Journal    
DOI: 10.1093/ije/28.4.711     Document Type: Article

References (57)

1. Loughna S, Bennett P, Moore G. Molecular analysis of the expression of transthyretin in intestine and liver from Trisomy 18 fetuses. Hum Genet 1995;95:89-95.
2. Ramesh K, Verma R. Parental origin of the extra chomosome 18 in Edwards syndrome. Ann Genet 1996;39:110-12.
3. Boss A, Broers C, Hazebrack F et al. Avoidance of emergency surgery in newborn infants with Trisomy 18. Lancet 1992;339:913-15.
4. Edwards J, Cameron A, Crosse V, Harnden D, Wolff O. A new trisomic syndrome. Lancet 1960;i:787-90.
5. Hecht F, Motulsky A, Gilbert E. The No 17-18 (E) Trisomy syndrome: studies on cytogenetics, dermatoglyphics, paternal age of linkage. J Pediatr 1963;63:605.
6. Cohen P, Erkman B. Frequency of occurrence of chromosomal syndromes 11, E Trisomy. Am J Hum Genet 1966;18:387-88.
7. Neilsen J, Holm V, Haahr J. Prevalence of Edwards' syndrome, clustering and seasonal variation. Hum Genet 1975;26:113-16.
8. Hook E, Porter I. Comments on Social Differences in Frequency of Chromosome Abnormalities Putative Clustering of Down's Syndrome and Radiation Studies in Population Cytogenetics. New York: Academic Press, 1977.
9. Hansmann I. Clustering of chromosomal aneuploidy and tracing of non-disjunction in man. Environ Health Perspect 1979;31:23-25.
10. de Grouchy J, Turean C. Trisomy 18 in Clinical Atlas of Human Chromosomes. New York: John Wiley, 1984, pp.290-323.
11. Anneren G. Incidence of trisomy 18 in Sweden in 1981-1982: clustering in a small region. Clin Genet 1986;26:345-47.
12. Young I, Cook J, Mehta L. Changing demography of trisomy 18. Arch Dis Child 1986;61:1035-36.
13. Heinrichs H, Allen W, Nielsen S. Simultaneous Trisomy 18 and Trisomy 21 cluster. Lancet 1963:ii:468.
14. Taylor A. Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau syndrome. J Med Genet 1968;5:227-52.
15. Hungerford DA. Leukocytes cultured from small inocula, the whole blood and the preparation of metaphase chromosomes by treatment with hypotonic potassium chloride. Stain Technol 1965;40:320.
16. Seabright M. A rapid banding technique for human chromosomes. Lancet 1971;ii:97.
17. Mitelman F. ISCN - An International System for Human Cytogenetics. Basle, Switzerland: Karger, 1995.
18. SPSS. Statistical Package for Social Sciences for Windows: User's Guide, Release 7.5. New York: McGraw Hill, 1995.
19. EPI Info. Public Domain Software for Epidemiology and Disease Surveillance, Version 6. Atlanta: Centers for Disease Control, Epidemiology Program Office, 1995.
20. Kirkwood P. Essentials of Medical Statistics. London: Blackwell Scientific Publications, 1988, pp. 128-30.
21. Armitage P, Berry G. Statistical Methods in Medical Research. Oxford: Blackwell Scientific Publications, 1991, p.324.
22. Moussa MAA, El-Sayed AM. Mortality in Kuwait: pattern and seasonality. Med Principles Pract 1998;7:18-27.
23. Goodman R, Gorlin R. Trisomy 18 in the Malformed Infant and Child. London: Oxford University Press, 1983, pp.120-21.
24. Jaruratanasirikul S, Jinorose U. An infant with double trisomy (48,XXX,+18). Am J Med Genet 1994;49:207-10.
25. Collins A, Fisher J, Crolla J, Cookwell A. Further case of trisomy 18 mosaicism with a mild phenotype. Am J Med Genet 1995; 56:121-22.
26. Smith D. Autosomal abnormalities. Am J Obstet Gynecol 1964;90: 1055-77.
27. Carter P, Pearn J, Bell J, Martin N, Anderson N. Survival in trisomy 18. Clin Genet 1985;27:59-61.
28. Schlessel J, Brown W, Lysikiewicz A, Schiff R, Zaslav A. Monozygotic twins with trisomy 18: a report of discordant phenotype. J Med Genet 1990;27:640-42.
29. Morosini P, Verdura C, Paolillo F, Fornari M, Argentiero M, Nelloni C. Trisomy 18 (Edwards' syndrome): two cases reports. Pediatr Med Chirurgico 1992;14:75-77.
30. Naguib K, Al-Awadi SA, Marafie M, Al-Hijji S. Trisomy 18 clustering in Kuwait. Clin Genet 1987;32:379-82.
31. Warkany J. Trisomy 18 in Congenital Malformations Notes and Comments. Chicago: Year Book Medical Publishers, 1981, pp.303-09.
32. Huether C, Martin R, Sloppelman S et al. Sex ratios in fetuses and liveborn infants with autosomal aneuploidy. Am J Med Genet 1996;63:492-500.
33. Adeyokunnu A. Autosomal trisomy 18 and 13 syndromes in Ibadan, Nigeria. Aft J Med Sci 1983;12:81-90.
34. Ya-gang X, Robinson W, Spiegel R, Binkert F, Ruefenucht U, Schinzel A. Parental origin of the supernumerary chromosome in trisomy 18. Clin Genet 1993;44:57-61.
35. Baty B, Jorde L, Blockburn B, Grey J. Natural history of trisomy 18 and trisomy 13: II, Psychomotor development. Am J Med Genet 1994;49:189-94.
36. Van Dyke D, Allen M. Clinical management consideration in long-term survivors with T18. Pediatrics 1990;85:753-59.
37. Holmes JM, Coates CM. Assessment of visual acuity in children with Trisomy 18. Ophthalmic Genet 1994;15:115-20.
38. Weber W, Manunes P, Day R, Miller P. Trisomy 17-18 (E): studies in long term survival with report of two autopsied cases. Pediatrics 1964;34:533.
39. Ozonoff M, Stunbach H, Manunes P. The trisomy 18 syndrome. Am J Roentgenol 1964;91:618.
40. Root S, Carey J. Survival in trisomy 18. Am J Med Genet 1994;49:170-74.
41. Dunin-Wasowicz D, Kragewska-Walasek M, Rowecka-Trzebicka K, Gurkaw-Molecho M., Gulkowska A, Chzanowska K. Diagnosis of Edwards syndrome in newborns. Pediatr Pol 1995;70:865-74.
42. Seulvedo W, Treadwell M, Fisk N. Prenatal detection of preaxial upper limb reduction in trisomy 18. Obstet Gynecol 1995;85:847-50.
43. Peer J, Braun J. Ocular pathology in trisomy 18 (Edwards syndrome). Ophtalmologie 1986;192:176-78.
44. Bacal D, Nelson L, Zackai E, Lavrich J, Kousseff B, McDonald-McGinn D. Ankyloblepharon filitome adonatum in trisomy 18. J Pediatr Ophthalmol Strabismus 1993;30:337-39.
45. Moore J, Wight N, Jones M, Krous H. Truncus arteriosus associated with trisomy 18. Pediatr Cardiol 1994;5:154-56.
46. Rogers R. Trisomy 18 with unilateral atypical ectroactyly. Am J Med Genet 1994;53:390-92.
47. Spencer K, Mullard A, Coombes E, Macri J. Prenatal screening for trisomy 18 with free beta human chorionic gonadotrophin as a marker. Br Med J 1993;307:1455-58.
48. Tanaka K, Uemoto S, Asonuma K et al. Hepatoblastoma in a 2 year old girl with trisomy 18. Eur J Ped Surg 1992;2:298-300.
49. Lee W, Hou J, Van K, Wang T. Trisomy 18 in a patient with CHARGE association. J Formos Med Assoc 1995;94:6-12.
50. Abba G, Zllweye H, Cuang R. Satellite association in familial mosaicism. Helv Paed Acta 1966;21:293-99.
51. Hsu L, Hirschhorn K, Goldstein A, Barcinski M. Familial chromosomal mosaicism, genetic aspects. Ann Hum Genet 1970;33:343-49.
52. Backer B, Carpenter A, Esposito M, Esposito R, Sandier L. The genetic controls of meiosis. Ann Rev Genet 1976;10:53-134.
53. Puri R, Khanna K, Bhargava I, Balakrishnan S. Role of consanguinity in chromosomal syndromes. Int J Med Res 1977;65:859-64.
54. Alfi O, Chang R, Azen S. Evidence for genetic control of nondisjunction in man. Am J Hum Genet 1980;31:477-83.
55. Naguib KK. Consanguinity and Chromosomal Aberrations. Thesis submitted for PhD degree in Human Genetics, Medical Research Institute, Alexandria University, Egypt, 1984.
56. Naguib K, Awadi S, Moussa M, Mohammed F. Down syndrome in sibs: a study of recessive hypothesis controlling non-disjunction. The Bull HI Public Health 1992;22:1.
57. Penrose L. Mongolism. Br Med Bull 1961;17:184-89.