Entry - #610189 - SENIOR-LOKEN SYNDROME 6; SLSN6 - OMIM
# 610189

SENIOR-LOKEN SYNDROME 6; SLSN6


Phenotype-Gene Relationships

Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
12q21.32 Senior-Loken syndrome 6 610189 AR 3 CEP290 610142
Clinical Synopsis
 
Phenotypic Series
 

INHERITANCE
- Autosomal recessive
HEAD & NECK
Eyes
- Tapetoretinal degeneration
- Decreased visual acuity
GENITOURINARY
Kidneys
- End stage renal disease
NEUROLOGIC
Central Nervous System
- No cerebellar vermis aplasia/hypoplasia
MISCELLANEOUS
- Allelic to Joubert syndrome 5 (610188) and Leber congenital amaurosis type X (610142)
MOLECULAR BASIS
- Caused by mutation in the 290-kD centrosomal protein gene (CEP290, 610142.0004).

TEXT

A number sign (#) is used with this entry because of evidence that Senior-Loken syndrome-6 (SLSN6) is caused by homozygous mutation in the NPHP6 gene (CEP290; 610142) on chromosome 12q21.

Mutations in the CEP290 gene can also cause Joubert syndrome-5 (610188).


Description

Senior-Loken syndrome-6 (SLSN6) is an autosomal recessive disorder characterized by the association of nephronophthisis resulting in end-stage renal disease in the second decade of life with retinal degeneration (Sayer et al., 2006).

For a phenotypic description and a discussion of genetic heterogeneity of Senior-Loken syndrome, see 266900.


Clinical Features

Sayer et al. (2006) described a Turkish family in which 2 sibs with Senior-Loken syndrome reached end-stage renal disease at 11 and 13 years of age, respectively. Both had tapetoretinal degeneration resulting in reduced vision before 3 years of age.


Inheritance

The transmission pattern of SLSN6 in the family reported by Sayer et al. (2006) was consistent with autosomal recessive inheritance.


Mapping

Identification of causative mutations in the CEP290 gene in the Turkish family with Senior-Loken syndrome described by Sayer et al. (2006) localized the SLSN6 phenotype to chromosome 12q21.32.


Molecular Genetics

In 2 affected sibs in a Turkish family segregating Senior-Loken syndrome, Sayer et al. (2006) detected a homozygous 5-bp deletion in the CEP290 gene (610142.0004). The mutation altered an obligatory splice site.


REFERENCES

  1. Sayer, J. A., Otto, E. A., O'Toole, J. F., Nurnberg, G., Kennedy, M. A., Becker, C., Hennies, H. C., Helou, J., Attanasio, M., Fausett, B. V., Utsch, B., Khanna, H., and 30 others. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nature Genet. 38: 674-681, 2006. [PubMed: 16682973, related citations] [Full Text]


Creation Date:
Anne M. Stumpf : 6/14/2006
alopez : 07/17/2023
carol : 01/17/2018
alopez : 06/14/2006

# 610189

SENIOR-LOKEN SYNDROME 6; SLSN6


ORPHA: 3156;   DO: 0050576;  


Phenotype-Gene Relationships

Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
12q21.32 Senior-Loken syndrome 6 610189 Autosomal recessive 3 CEP290 610142

TEXT

A number sign (#) is used with this entry because of evidence that Senior-Loken syndrome-6 (SLSN6) is caused by homozygous mutation in the NPHP6 gene (CEP290; 610142) on chromosome 12q21.

Mutations in the CEP290 gene can also cause Joubert syndrome-5 (610188).


Description

Senior-Loken syndrome-6 (SLSN6) is an autosomal recessive disorder characterized by the association of nephronophthisis resulting in end-stage renal disease in the second decade of life with retinal degeneration (Sayer et al., 2006).

For a phenotypic description and a discussion of genetic heterogeneity of Senior-Loken syndrome, see 266900.


Clinical Features

Sayer et al. (2006) described a Turkish family in which 2 sibs with Senior-Loken syndrome reached end-stage renal disease at 11 and 13 years of age, respectively. Both had tapetoretinal degeneration resulting in reduced vision before 3 years of age.


Inheritance

The transmission pattern of SLSN6 in the family reported by Sayer et al. (2006) was consistent with autosomal recessive inheritance.


Mapping

Identification of causative mutations in the CEP290 gene in the Turkish family with Senior-Loken syndrome described by Sayer et al. (2006) localized the SLSN6 phenotype to chromosome 12q21.32.


Molecular Genetics

In 2 affected sibs in a Turkish family segregating Senior-Loken syndrome, Sayer et al. (2006) detected a homozygous 5-bp deletion in the CEP290 gene (610142.0004). The mutation altered an obligatory splice site.


REFERENCES

  1. Sayer, J. A., Otto, E. A., O'Toole, J. F., Nurnberg, G., Kennedy, M. A., Becker, C., Hennies, H. C., Helou, J., Attanasio, M., Fausett, B. V., Utsch, B., Khanna, H., and 30 others. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nature Genet. 38: 674-681, 2006. [PubMed: 16682973] [Full Text: https://doi.org/10.1038/ng1786]


Creation Date:
Anne M. Stumpf : 6/14/2006

Edit History:
alopez : 07/17/2023
carol : 01/17/2018
alopez : 06/14/2006