Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis.
Pediatr Nephrol
; 38(1): 119-129, 2023 01.
Article
in En
| MEDLINE
| ID: mdl-35445972
ABSTRACT
BACKGROUND:
Nephropathic cystinosis is an autosomal recessive disease caused by a mutation in the CTNS gene which encodes cystinosin, a lysosomal cystine transporter. The spectrum of mutations in the CTNS gene is not well defined in the North African population. Here, we investigated twelve patients with nephropathic cystinosis belonging to eight Tunisian families in order to analyze the clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis.METHODS:
Clinical data were collected retrospectively. Molecular analysis of the CTNS gene was performed by Sanger sequencing.RESULTS:
We describe a new splicing mutation c.971-1G > C in the homozygous state in 6/12 patients which seems to be a founder mutation. The reported deletion of 23nt c.771_793 Del (p.Gly258Serfs*30) was detected in a homozygous state in one patient and in a heterozygous compound state with the c.971-1G > C mutation in 3/12 patients. Two of 12 patients have a deletion of exons 4 and 5 of the CTNS gene. None of our patients had the most common 57-kb deletion.CONCLUSIONS:
The mutational spectrum in the Tunisian population is different from previously described populations. Thus, a molecular diagnostic strategy must be implemented in Tunisia, by targeting as a priority the common mutations described in this country. Such a strategy will allow a cost-effective diagnosis confirmation as well as early administration of treatment with oral cysteamine. A higher resolution version of the Graphical abstract is available as Supplementary information.Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Cystinosis
/
Amino Acid Transport Systems, Neutral
Limits:
Child
/
Humans
Language:
En
Journal:
Pediatr Nephrol
Year:
2023
Document type:
Article