Senior-Loken syndrome 3 is an autosomal recessive disorders caused by mutations of the NPHP3 gene. It is characterized by medullary cysts and progressive renal failure and Leber congenital amaurosis.
| 1. |
Boichis H et al. (1973) Congenital hepatic fibrosis and nephronophthisis. A family study.
|
| 2. |
Fairley KF et al. (1963) Familial Visual Defects Associated with Polycystic Kidney and Medullary Sponge Kidney.
|
| 3. |
None (1924) The Inheritance of a Retinal Abnormality in White Mice.
|
| 4. |
Otto EA et al. (2005) Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin.
|
| 5. |
SENIOR B et al. (1961) Juvenile familial nephropathy with tapetoretinal degeneration. A new oculorenal dystrophy.
|
| 6. |
LOKEN AC et al. (1961) Hereditary renal dysplasia and blindness.
|
| 7. |
Olbrich H et al. (2003) Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.
|
| 8. |
Otto E et al. (2002) A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution.
|
| 9. |
Schuermann MJ et al. (2002) Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36.
|
| 10. |
Omran H et al. (2002) Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 gene.
|
| 11. |
Caridi G et al. (1998) Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus.
|
| 12. |
Warady BA et al. (1994) Senior-Loken syndrome: revisited.
|
| 13. |
Antignac C et al. (1993) A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p.
|
| 14. |
Mendley SR et al. (1995) Hereditary sclerosing glomerulopathy in the conorenal syndrome.
|
| 15. |
None (1969) Hereditary renal-retinal dysplasia.
|
| 16. |
Bois E et al. (1970) [Association of chronic tubulo-interstitial nephropathy and of tapeto-retinal degeneration. Genetic study].
|
| 17. |
Fontaine JL et al. (1970) [Tubulo-interstitial nephropathy in children with tapeto-retinal degeneration (Senior's syndrome. (1 case)].
|
| 18. |
None (1969) Familial occurrence of congenital retinal blindness and developmental renal lesions.
|
| 19. |
Schuman JS et al. (1985) Senior-Loken syndrome (familial renal-retinal dystrophy) and Coats' disease.
|
| 20. |
Clarke MP et al. (1992) Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness.
|
| 21. |
Proesmans W et al. (1975) Nephronophthisis and tapetoretinal degeneration associated with liver fibrosis.
|
| 22. |
Hogewind BL et al. (1977) Electro-rentinal abnormalities in heterozygotes of renal-retinal dysplasia.
|
| 23. |
Avasthi PS et al. (1976) Hereditary renal-retinal dysplasia and the medullary cystic disease-nephronophthisis complex.
|
| 24. |
Diekmann L et al. (1977) [Familial nephropathy with retinitis pigmentosa and peripheral dysostosis].
|
| 25. |
Godel V et al. (1979) Retinal manifestations in familial juvenile nephronophthisis.
|
| 26. |
Khanna H et al. (2009) A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
|
| 27. |
OMIM.ORG article Omim 606995
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