Rett syndrome: Geographic variation in prevalence in Norway

Brain and Development

Volumn 19, Issue 4, 1997, Pages 258-261

  Skjeldal, Ola H ^a   Von Tetzchner, Stephen ^a   Aspelund, Finn ^b   Herder, Gyro Aas ^c   Lofterød, Bjørn ^d  

^a UNIVERSITY OF OSLO   (Norway)

^b ØSterlide Habilitation Centre   (Norway)

^c NORDLAND HOSPITAL   (Norway)

^d Furutun Habilitation Centre   (Norway)

Author keywords

Epidemiology; Norway; Rett syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; FEMALE; GEOGRAPHIC DISTRIBUTION; HEALTH CARE QUALITY; HEALTH CARE SYSTEM; HUMAN; NORWAY; RETT SYNDROME;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; GEOGRAPHY; HUMANS; NORWAY; PREVALENCE; RETT SYNDROME;

EID: 0030962950     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(97)00572-X     Document Type: Article

References (18)

1. Rett A. Über ein ergenartiges hirnatrophisches Syndrome bei Hyperammonamie im Kindesalter (On an unusal brain atrophy syndrome with hyperammonemia in childhood). Wien. Med. Wochenschr. 1966; 116: 723-726.
2. Hagberg B. Rett syndrome: Swedish approach to analysis of prevalence and cause. Brain Dev. 1985; 7: 277-280.
3. Kerr AM, Stephenson JBP. Rett's syndrome in the West of Scotland. Br. Med. J. 1985; 291: 579-582.
4. Kerr AM. Early clinical signs in the Rett disorder. Neuropediatrics 1995; 26: 67-71.
5. Boltshauser E, Kunze C. Prevalence of Rett syndrome in Switzerland. Helv. Paediatr. Acta 1987; 42: 407-411.
6. Burd L, Vesley B, Martsolf JT, Kerbeshian J. Prevalence study of Rett syndrome in North Dakota children. Am. J. Med. Genet. 1991; 38: 565-568.
7. Kozinets CA, Skender ML, MacNaughton N et al. Epidemiology of Rett syndrome: a population-based registry. Pediatrics, 1993; 91: 445-450.
8. Terai K, Munesue T, Hiratani M, Zheng-Yan J, Jibiki I, Yamaguchi N. The prevalence of Rett syndrome in Fukui prefecture. Brain Dev. 1995; 17: 153-154.
9. Talvik T, Søøt A, Beilman A, Soopold T, Nurk K. Rett syndrome in Estonia: prevalence of the classical phenotype. Acta Pædiatr. 1995; 84: 1070-1071.
10. Âkesson HO, Hagberg B, Wahlstrøm J, Witt-Engerström I. Rett syndrome: a search for gene sources. Am. J. Med. Genet. 1992; 42: 104-110.
11. Hagberg B. Rett syndrome: clinical peculiarities and biological mysteries. Acta Pædiatr. 1995; 84: 971-976.
12. Hagberg B, Skjeldal OH. Rett variant: a suggested model for inclusion criteria. Pediatr. Neurol. 1994; 11: 5-11.
13. Trevathan E, Moser HW. Diagnostic criteria for Rett syndrome. Ann. Neurol. 1988; 23: 425-428.
14. von Tetzchner S, Jacobsen KA, Smith L, Skjeldal OH, Heiberg A, Fagan JF. Vision, cognition and developmental characteristics among girls and women with Rett Syndrome. Dev. Med. Child. Neurol. 1996; 38: 212-225.
15. Hesselberg F, von Tetzchner S. Organisering av tjenester og samarbeid (Organization of services and collaboration). In: von Tetzchner S et al., editors. Habilitering - Tverrfaglig Arbeid For Mennesker Med Medfødte Og Tidlig Ervervede Funksjonshemninger. Oslo: Ad Notam Gyldendal, 1992: 20-46.
16. Witt Engerstrøm I. Evaluation of clinical signs. In: Hagberg B, editor. Rett Syndrome - Clinical and Biological Aspects. Clinics in Developmental Medicine, No. 127. London: Mac Keith Press, 1993: 26-39.
17. Anvret M, Zhang ZP. Current status of genetic research in Rett syndrome. Neuropediatrics 1995; 26: 88-89.
18. Hagberg B, Anvret M, Percy A, Wahlstrøm J. Conclusion: aspects on origin-future approach. In: Hagberg B, editor. Rett Syndrome - Clinical And Biological Aspects. Clinics in Developmental Medicine, No. 127. London: Mac Keith Press, 1993: 111-116.