Literature DB >> 19657313

Case report: severe neonatal hyperkalemia due to pseudohypoaldosteronism type 1.

Bahareh Schweiger1, Margaret W Moriarty, Melissa A Cadnapaphornchai.   

Abstract

Hyponatremia and hyperkalemia in infancy can represent a variety of renal and genetic disorders with significant long-term health implications. We report a newborn with severe hyperkalemia and hyponatremia from autosomal recessive pseudohypoaldosteronism type 1 requiring aggressive therapy. The evaluation and treatment of children with disorders of mineralocorticoid action are discussed.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19657313     DOI: 10.1097/MOP.0b013e328325a55f

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  4 in total

1.  Ocular and skin manifestations in systemic pseudohypoaldosteronism.

Authors:  Mahmoud Salah Eliwa; Aymen Hussein El-Emmawie; Mahmood Ahmad Saeed
Journal:  BMJ Case Rep       Date:  2014-03-20

2.  Phenotypic variation of autosomal recessive pseudohypoaldosteronism type I: a case in point.

Authors:  Gunjeet Kala Ahluwalia; Majed Dasouki; Angela Lennon
Journal:  Clin Case Rep       Date:  2014-09-15

3.  Systemic Pseudohypoaldosteronism Type I: A Case Report and Review of the Literature.

Authors:  Nasifa Nur; Cameron Lang; Juanita K Hodax; Jose Bernardo Quintos
Journal:  Case Rep Pediatr       Date:  2017-04-18

4.  Novel mutations in the SCNN1A gene causing Pseudohypoaldosteronism type 1.

Authors:  Jian Wang; Tingting Yu; Lei Yin; Jing Li; Li Yu; Ye Shen; Yongguo Yu; Yongnian Shen; Qihua Fu
Journal:  PLoS One       Date:  2013-06-06       Impact factor: 3.240

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.