Literature DB >> 25326109

Common mutation causes cystinosis in the majority of black South African patients.

E Patricia Owen1, Jenisha Nandhlal, Felicity Leisegang, George Van der Watt, Peter Nourse, Priya Gajjar.   

Abstract

BACKGROUND: The mutations responsible for cystinosis in South African patients are currently unknown. A pertinent question is whether they are similar to those described elsewhere in the world.
METHODS: Children who were being managed for cystinosis in the Western Cape Province of South Africa between 2002 and 2013 were studied. All underwent molecular analysis to detect sequence variations in the cystinosis gene.
RESULTS: This cohort study included 20 patients, 13 of whom were Xhosa-speaking black South Africans and seven were Cape Coloureds (mixed race); none were Caucasian. All had nephropathic infantile-type cystinosis with evidence of proximal tubulopathy, with glycosuria and renal phosphate wasting. Diagnosis was confirmed in 19 cases by demonstrating an elevated cystine concentration in leukocytes. Molecular analysis of the cystinosin gene revealed that 19 patients had a G > A mutation in intron 11 (CTNS-c.971-12G > A p.D324AfsX44) which caused an out-of-frame 10-bp insertion. Of these 19 patients, 16 were homozygous for this mutation, which was the most frequent mutation identified in the alleles of the black South African and Cape Coloured patients (96 and 71 %, respectively).
CONCLUSION: We recommend that black South African and Cape Coloured patients presenting with cystinosis be tested for CTNS-c.971-12G > A in the first instance, with the possibility of prenatal testing being offered to at-risk families.

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Year:  2014        PMID: 25326109     DOI: 10.1007/s00467-014-2980-7

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  28 in total

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2.  Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS).

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3.  Mutational Spectrum of the CTNS Gene in Egyptian Patients with Nephropathic Cystinosis.

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4.  CTNS mutations in an American-based population of cystinosis patients.

Authors:  V Shotelersuk; D Larson; Y Anikster; G McDowell; R Lemons; I Bernardini; J Guo; J Thoene; W A Gahl
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

5.  Identification of 14 novel CTNS mutations and characterization of seven splice site mutations associated with cystinosis.

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Journal:  Hum Mutat       Date:  2002-12       Impact factor: 4.878

6.  Nephropathic cystinosis in adults: natural history and effects of oral cysteamine therapy.

Authors:  William A Gahl; Joan Z Balog; Robert Kleta
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7.  Molecular pathogenesis of cystinosis: effect of CTNS mutations on the transport activity and subcellular localization of cystinosin.

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10.  An integrated map of genetic variation from 1,092 human genomes.

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  6 in total

1.  Molecular Analysis of the CTNS Gene in Indians with Nephropathic Cystinosis.

Authors:  Anup Arunrao Deshpande; Rajan Ravichandran; Anand Kumar Bachhawat
Journal:  Indian J Pediatr       Date:  2016-11-25       Impact factor: 1.967

Review 2.  The renal Fanconi syndrome in cystinosis: pathogenic insights and therapeutic perspectives.

Authors:  Stephanie Cherqui; Pierre J Courtoy
Journal:  Nat Rev Nephrol       Date:  2016-12-19       Impact factor: 28.314

3.  Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis.

Authors:  Mariem El Younsi; Médiha Trabelsi; Sandra Ben Youssef; Inès Ouertani; Yousra Hammi; Ahlem Achour; Faouzi Maazoul; Maher Kharrat; Tahar Gargah; Ridha M'rad
Journal:  Pediatr Nephrol       Date:  2022-04-20       Impact factor: 3.714

4.  Pitfalls of relying on genetic testing only to diagnose inherited metabolic disorders in non-western populations - 5 cases of pyruvate dehydrogenase deficiency from South Africa.

Authors:  Surita Meldau; Carl Fratter; Louisa Ntombenhle Bhengu; Kate Sergeant; Kashief Khan; Gillian Tracy Riordan; Peter Allan Minham Berman
Journal:  Mol Genet Metab Rep       Date:  2020-07-22

Review 5.  Newborn Screening: Review of its Impact for Cystinosis.

Authors:  Katharina Hohenfellner; Ewa Elenberg; Gema Ariceta; Galina Nesterova; Neveen A Soliman; Rezan Topaloglu
Journal:  Cells       Date:  2022-03-25       Impact factor: 6.600

Review 6.  Paediatric Nephrology in Africa.

Authors:  Christopher I Esezobor; Adebimpe E Alakaloko; Bashir Admani; Rashid Ellidir; Peter Nourse; Mignon I McCulloch
Journal:  Curr Pediatr Rep       Date:  2021-10-25
  6 in total

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