Literature DB >> 16021385

Sudden cardiac arrest in a neonate with congenital adrenal hyperplasia.

S Agarwal1, G Deshpande, D Agarwal, A Dave, J J Shah.   

Abstract

We describe a 6-day-old male who developed cardiac arrest due to hyperkalemia secondary to congenital adrenal hyperplasia and was successfully resuscitated. This case illustrates the importance of considering congenital adrenal hyperplasia as one of the causes of sudden cardiac arrest in a neonate. A literature review revealed only one similar case in a 3-month-old with a fatal outcome.

Entities:  

Mesh：

Year:  2005        PMID： 16021385     DOI： 10.1007/s00246-004-0858-3

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN： 0172-0643            Impact factor:   1.655


  13 in total

Review 1.  Congenital adrenal hyperplasia.

Authors:  Phyllis W Speiser; Perrin C White
Journal:  N Engl J Med       Date:  2003-08-21       Impact factor: 91.245

Review 2.  Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology.

Authors: 
Journal:  J Clin Endocrinol Metab       Date:  2002-09       Impact factor: 5.958

3.  Newborn screening for 21-hydroxylase deficiency: results of CYP21 molecular genetic analysis.

Authors:  S F Witchel; S Nayak; M Suda-Hartman; P A Lee
Journal:  J Pediatr       Date:  1997-08       Impact factor: 4.406

4.  Prenatal diagnosis of 21-hydroxylase deficiency by the complementary deoxyribonucleic acid probe for cytochrome P-450C-21OH.

Authors:  R H Reindollar; J B Lewis; P C White; P M Fernhoff; P G McDonough; J B Whitney
Journal:  Am J Obstet Gynecol       Date:  1988-03       Impact factor: 8.661

Review 5.  Clinical review 54: Genetics, diagnosis, and management of 21-hydroxylase deficiency.

Authors:  W L Miller
Journal:  J Clin Endocrinol Metab       Date:  1994-02       Impact factor: 5.958

Review 6.  Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  P C White; P W Speiser
Journal:  Endocr Rev       Date:  2000-06       Impact factor: 19.871

7.  First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.

Authors:  E Mornet; J Boue; M Raux-Demay; P Couillin; J F Oury; Y Dumez; J Dausset; D Cohen; A Boué
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

8.  Cardiac arrest in an infant with congenital adrenal hyperplasia.

Authors:  W Ruppen; N Hagenbuch; M Jöhr; P Christen
Journal:  Acta Anaesthesiol Scand       Date:  2003-01       Impact factor: 2.105

9.  Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid.

Authors:  B Gueux; J Fiet; P Couillin; M C Raux-Demay; E Mornet; H Galons; J M Villette; J Boue; C Dreux
Journal:  J Clin Endocrinol Metab       Date:  1988-03       Impact factor: 5.958

Review 10.  Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene.

Authors:  R C Wilson; J Q Wei; K C Cheng; A B Mercado; M I New
Journal:  J Clin Endocrinol Metab       Date:  1995-05       Impact factor: 5.958
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.