Literature DB >> 16030166

Mutations in CYP11B1 and congenital adrenal hyperplasia in Moroccan Jews.

Tamar Paperna1, Ruth Gershoni-Baruch, Kader Badarneh, Leah Kasinetz, Ze'ev Hochberg.   

Abstract

CONTEXT: In Jews of Moroccan descent (MJ), the prevalence of steroid 11beta-hydroxylase deficiency (11-OHD) is relatively high, with a carrier rate estimated as approximately one in 40. A single mutation in the CYP11B1 gene (encoding 11beta-hydroxylase), R448H, was suggested to account for the disease alleles in this population. STUDY
SUBJECTS: We screened 236 healthy MJ for R448H.
RESULTS: Only two of the subjects screened were found to be carriers, suggesting that the R448H allele frequency is lower than was assumed previously. An R448H/R448C compound heterozygote patient, diagnosed with 11-OHD, was identified. However, a subsequent screen of MJ subjects for R448C failed to detect any carriers, suggesting that this was a private mutation of this family.
CONCLUSION: The high incidence of 11-OHD in MJ, therefore, is only partially explained by the presence of R448H as a founder mutation.

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Year:  2005        PMID: 16030166     DOI: 10.1210/jc.2005-1145

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  7 in total

1.  Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11beta-hydroxylase deficiency.

Authors:  S Cingöz; B Ozkan; H Döneray; M Sakizli
Journal:  J Endocrinol Invest       Date:  2007-04       Impact factor: 4.256

2.  Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X.

Authors:  Audrey Mary Matallana-Rhoades; Juan David Corredor-Castro; Francisco Javier Bonilla-Escobar; Bony Valentina Mecias-Cruz; Liliana Mejia de Beldjena
Journal:  Colomb Med (Cali)       Date:  2016-09-30

3.  Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other.

Authors:  Katja Dumic; Robert Wilson; Pavinee Thanasawat; Zorana Grubic; Vesna Kusec; Katarina Stingl; Maria I New
Journal:  Eur J Pediatr       Date:  2009-12-22       Impact factor: 3.183

4.  Improving the diagnosis of 11β-hydroxylase deficiency using home-made MLPA probes: identification of a novel chimeric CYP11B2/CYP11B1 gene in a Sicilian patient.

Authors:  S Menabò; S Boccassini; A Gambineri; A Balsamo; R Pasquali; O Prontera; L Mazzanti; L Baldazzi
Journal:  J Endocrinol Invest       Date:  2015-08-18       Impact factor: 4.256

5.  Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11 β -Hydroxylase Deficiency.

Authors:  Katja Dumic; Tony Yuen; Zorana Grubic; Vesna Kusec; Ingeborg Barisic; Maria I New
Journal:  Int J Endocrinol       Date:  2014-06-02       Impact factor: 3.257

6.  Fetal anogenital distance using ultrasound.

Authors:  Ezra Aydin; Rosemary Holt; Daren Chaplin; Rebecca Hawkes; Carrie Allison; Gerald Hackett; Topun Austin; Alex Tsompanidis; Lidia Gabis; Shimrit Ilana Ziv; Simon Baron-Cohen
Journal:  Prenat Diagn       Date:  2019-05-10       Impact factor: 3.050

Review 7.  Genetics of congenital adrenal hyperplasia.

Authors:  Nils Krone; Wiebke Arlt
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2009-04       Impact factor: 4.690

  7 in total

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