Congenital hydrocephalus in 1961-2000: Incidence, prenatal diagnosis and prevalence according to maternal age;Vrozeny̌ hydrocefalus v období 1961-2000 - Výskyt, prenatální diagnostika a prevalence podle věku matky

Ceska Gynekologie

Volumn 67, Issue 6, 2002, Pages 360-364

  Sipek A ^a   Gregor, V ^a   Horacek J ^a   Masatova D ^a  

^a NONE

Author keywords

Birth defect; Congenital hydrocephalus; Czech; Incidence

Indexed keywords

ARTICLE; BIRTH DEFECT; CONGENITAL HYDROCEPHALUS; CZECH REPUBLIC; EPIDEMIOLOGICAL DATA; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MATERNAL AGE; MATHEMATICAL ANALYSIS; NEWBORN; PRENATAL DIAGNOSIS; PREVALENCE; RISK FACTOR; STATISTICAL ANALYSIS; FEMALE; HYDROCEPHALUS; PREGNANCY;

CZECH REPUBLIC; FEMALE; HUMANS; HYDROCEPHALUS; INCIDENCE; INFANT, NEWBORN; MATERNAL AGE; PREGNANCY; PRENATAL DIAGNOSIS; PREVALENCE;

EID: 0036883254     PISSN: 12107832     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)

1. Annual Report 2000 of the International Clearinghouse for Birth Defects Monitoring Systems (ICBDMS) with data for 1998, 2000, s 52-106.
2. Bamforth, S. J., Baird, P. A.: Spina bifida and hydrocephalus: A population study over 35-year-period. Am. J. Med. Genet., 44, 1989, s. 225-230.
3. Bergsma, D.: Birth Defects Compendium. National Foundation - March of Dimes by the Macmillan Press Ltd. 1989.
4. Blackburn, B. L., Fineman, R. M.: Epidemiology of congenital hydrocephalus in Utah, 1940-1979: report of an iatrogenically related "epidemic". Am. J. Med. Genet., 15, 1994, 52, 2, s. 123-129.
5. Bremer, F. A., Wanders, R. J. A., Schutgens, R. B. J.: VACTERL and hydrocephalus. Am. J. Med. Genet., 37, 1990, s. 425-426,
6. European Registration of Congenital Anomalies (EUROCAT) Report 7: 15 Years of Surveillance of Congenital Anomalies in Europe, 1980-1994. Institute of Hygiene and Epidemiology, Brussels 1997.
7. Glinianaia, S. V., Rankin, J.: Congenital hydrocephalus: occurrence and outcome. A population-based study in the North of England, 1985-1996. Northern Congenital Abnormality Survey Steering Group. Eur. J. Pediatr. Surg., 1999, 9, Suppl, s. 1-46.
8. Hájek, Z., Kulovaný, E., Macek, M.: Základy prenatální diagnostiky. Grada Publishing, Praha 2000.
9. Haverkamp, F., Wolfle, J., Aretz, M. et al.: Congenital hydrocephalus internus and aquaeduct stenosis: aetiology and implications for genetic counselling. Eur. J. Pediatr., 158, 1999, 6, s. 474-478.
10. Persaud, T. V. N., Persaud, M. P.: Central Nervous System and Craniofacial malformations. Advances in the Study of Birth Defects, 7. Alan R. Liss, Inc, New York 1982, s. 1-74.
11. Rajab, A., Vaishnav, A., Freeman, N. V., Patton, M. A.: Neural tube defects and congenital hydrocephalus in the Sultanate of Oman. J. Trop. Pediatr., 44, 1998, 5, s. 300-303.
12. Schrander-Stumpel, C., Fryns, J. P.: Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling. Eur. J. Pediatr., 157, 1998, 5, s. 355-362.
13. Stoll, C., Alembik, Y., Dott, B., Roth, M. P.: An epidemiologic study of environmental and genetic factors in congenital hydrocephalus. Eur. J. Epidemiol., 8, 1992, 6, s. 797-803.
14. Šípek, A., Gregor, V., Chudobová, M., Korandová, M.: Výskyt vrozených vad a úspéšnost prenatální diagnostiky v ČR v roce 1996. Čs. Pediatrie, 53, 1998, s. 704-710.
15. Šípek, A., Gregor, V., Chudobová, M., Korandová, M.: Výskyt vrozených vad a úspěšnost prenatální diagnostiky v ČR v roce 1997. Čs. Pediatrie, 54, 1999, s. 443-449.
16. Šípek, A., Gregor, V., Chudobová, M.: Výskyt vrozených vad a úspěšnost prenatální diagnostiky v ČR v roce 1998. Čs. Pediatrie, 55, 8, 2000, s. 518-524.
17. Šísek, A., Gregor, V., Horáček, J., Chudobová, M., Korandová M., Skibová, J.: Vy̌skyt kongenitálního hydrocefalu v ČR v období 1961-1995. Čes. Gynek., 63, 1998, s. 207-210.
18. Šípek, A.: Výskyt vrozených vad ve vybraných oblastech a státech světa v obdobf 1988-1998. Čes. Gynek., 67, 2002, s. 202-209.
19. Varadi, V., Toth, Z., Török, O., Papp, Z.: Heterogenity and recurrence risk for congenital hydrocephalus (ventriculomegaly): A prospective study. Am. J. Med. Genet., 29, 1988, s. 305-310.
20. Verhagen, W. I., Bartels, R. H., Fransen, E., van Camp, G., Renier, W. O., Grotenhuis, J. A.: Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression. J. Neurol. Sci., 11, 1998, 158, 1, s. 101-105.
21. Worldwide Congenital Malformations. A report from the International Clearinghouse for Birth Defects Monitoring System. Elsevier, Oxford 1991, s. 107-112.