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KOMPLİKE TİP HEREDİTER SPASTİK PARAPLEJİLİ BİR AİLE SUNUMU

Report of family with hereditary spastic paraplegia complicated type

Journal Name:

  • İnönü Üniversitesi Tıp Fakültesi Dergisi

Publication Year:

  • 2000

Key Words:

Keywords (Original Language):

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Hereditary spastic paraplegia (HSP) is a disease which can start at childhood ages and show heterogenous features. Besides, HSP has autosomal dominant, autosomal recessive and X linked transmission In this paper, a family with HSP with autosomal ressive transmission has been presented.
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Abstract (Original Language): 
Herediter spastik parapleji(HSP)heterojen özellik gösteren, çocukluk çağlarında başlayabilen bir hastalıktır. HSP dominant geçişli olmakla birlikte otozomal resesit ve X'e bağlı geçişleri de vardır. Bu yazıda otozomal resesif geçişli olduğu görülen HSP' li olgulara sahip bir aile sunulmuştur.
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  • 2
163-165
  • Turkish

REFERENCES

References: 

1. Walter G. Bradley. Neurology in Clinical Pratice; 2th Ed New York: Butterworth- Heinemann 1996: 1824- 1828.
2. Victor A, Mc Kusick MD. Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes. London: The Johns Hopkins Univesity Press Volume I 1992:1018- 1019.
3. Rowland LP. Hereditary and acquired spastic paraplegia in: Merritt's Textbook of Neurology, Rowland LP ( ed ). London: William- Wilkins 1995: 742- 749.
4. Ülkü A, Karasoy H, Araç N. ve ark. Herediter spastik parapleji. Nörolojik Bilimler Dergisi 1990; 7: 3- 4.
5.
Özere
n A, Sarıca Y. Herediter Serebellar Ataksiler ve Spastik paraplejiler. Çukurova Nörolojik Bilimler Derneği Yayınları 1994; 1: 2- 8.
6. Harding AE. Classification of hereditary ataxias and paraplegias. Lancet 1983; 1151- 1153.
7. Hedera P, Diamouro S, Monilla E. et al. Phenotypic analysis of autosomal dominant hereditary spastic paraplegia- linked to choromosome 8q. Neurology 1999; 53: 44- 50.
8. Paterrote C, Rudnicki D, Fizames C. et al. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q. Genome- Res 1998; 8: 1216- 1227.
9. Tomiyosu H, Hayashi R, Watanabe R. et al. A case of autosomal dominant, pure form spastic paraplegia with thinning of the corpus collosum. Rinsho Shinkeiqaku 1998; 38: 435- 439.
10. Veda M, Katayama Y, Kamiya Y. et al. Hereditary spastic paraplegia with a thin corpus callosum and thalamic involvement in Japan. Neurology 1998; 51: 1751- 1754.
11. Webb S, Flanagan N, Callaghan N. et al. A family with hereditary spastic paraparesis and epilepsy. Epilepsia 1997; 38: 495- 499.
12. Murray NMF. Motor evoked potentialsed. İn: Electrodiagnosis Clinical Neurology. Aminoff MJ (ed) 3th ed. New York: Churchill Livingstone 1992: 605- 626.

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