Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing

. 2016 Sep ; 175 (9) : 1199-1207. [epub] 20160818

Jazyk angličtina Země Německo Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid27539621
Odkazy

PubMed 27539621
DOI 10.1007/s00431-016-2759-x
PII: 10.1007/s00431-016-2759-x
Knihovny.cz E-zdroje

UNLABELLED: Familial neurohypophyseal diabetes insipidus (FNDI) is a rare hereditary disorder with unknown prevalence characterized by arginine-vasopressin hormone (AVP) deficiency resulting in polyuria and polydipsia from early childhood. We report the clinical manifestation and genetic test results in seven unrelated kindreds of Czech or Slovak origin with FNDI phenotype. The age of the sign outset ranged from 2 to 17 years with remarkable interfamilial and intrafamilial variability. Inconclusive result of the fluid deprivation test in three children aged 7 and 17 years old might cause misdiagnosis; however, the AVP gene analysis confirmed the FNDI. The seven families segregated together five different mutations, two of them were novel (c.164C > A, c.298G > C). In addition, DNA analysis proved mutation carrier status in one asymptomatic 1-year-old infant. CONCLUSIONS: The present study together with previously published data identified 38 individuals with FNDI in the studied population of 16 million which predicts a disease prevalence of 1:450,000 for the Central European region. The paper underscores that diagnostic water deprivation test may be inconclusive in polyuric children with partial diabetes insipidus and points to the clinical importance and feasibility of molecular genetic testing for AVP gene mutations in the proband and her/his first degree relatives. WHAT IS KNOWN: • At least 70 different mutations were reported to date in about 100 families with neurohypophyseal diabetes insipidus (FNDI), and new mutations appear sporadically. What is New: • Two novel mutations of the AVP gene are reported • The importance of molecular testing in children with polyuria and inconclusive water deprivation test is emphasized.

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J Clin Invest. 1993 Jun;91(6):2565-71 PubMed

Clin Endocrinol (Oxf). 2003 Jan;58(1):108-10 PubMed

Clin Endocrinol (Oxf). 2008 Dec;69(6):926-30 PubMed

Semin Nephrol. 2006 May;26(3):209-23 PubMed

J Am Soc Nephrol. 1999 Sep;10(9):1958-64 PubMed

Pituitary. 2015 Dec;18(6):898-904 PubMed

Science. 1980 Jan 25;207(4429):373-8 PubMed

Clin Endocrinol (Oxf). 2005 Aug;63(2):207-16 PubMed

J Clin Endocrinol Metab. 1997 Jan;82(1):51-6 PubMed

Open Neuroendocrinol J. 2011;4:136-146 PubMed

Clin Endocrinol (Oxf). 2012 Oct;77(4):586-92 PubMed

Klin Padiatr. 2013 Dec;225(7):407-12 PubMed

Eur J Endocrinol. 2015 Apr;172(4):461-72 PubMed

Cell Death Dis. 2014 Mar 27;5:e1148 PubMed

J Clin Endocrinol Metab. 1994 Aug;79(2):421-7 PubMed

Horm Res. 2003;60(3):143-7 PubMed

Exp Physiol. 2014 Jan;99(1):66-71 PubMed

Trends Endocrinol Metab. 1997 Nov;8(9):363-72 PubMed

Horm Res Paediatr. 2016;85(4):283-7 PubMed

Eur J Hum Genet. 2004 Jan;12(1):44-51 PubMed

J Endocrinol Invest. 2016 Mar;39(3):285-90 PubMed

Pediatr Nephrol. 2002 Dec;17(12):1063-5 PubMed

Ann Clin Lab Sci. 2015 Fall;45(5):588-92 PubMed

Pituitary. 2013 Jun;16(2):152-7 PubMed

J Clin Endocrinol Metab. 1993 Sep;77(3):599A-599G PubMed

Pituitary. 2012 Dec;15 Suppl 1:S1-5 PubMed

J Clin Invest. 1997 Apr 15;99(8):1897-905 PubMed

Endocrinol Diabetes Metab Case Rep. 2013;2013:130068 PubMed

Clin Genet. 2013 Jan;83(1):44-52 PubMed

J Clin Endocrinol Metab. 1999 Aug;84(8):2933-41 PubMed

Am J Hum Genet. 1996 Jan;58(1):107-17 PubMed

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