Literature DB >> 33025205

Incidental chronic kidney disease in an obese child with high myopia: Answers.

Aliza Mittal1, Manjesh Jayappa2, Binit Sureka3, Kuldeep Singh2.   

Abstract

Entities:  

Keywords:  Child; Chronic kidney disease; Claudin19 mutation; FHHNC 2; Familial hypomagnesemia with hypercalciuria and nephrocalcinosis; Myopia; Nephrocalcinosis

Year:  2020        PMID： 33025205     DOI： 10.1007/s00467-020-04785-z

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


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  3 in total

1.  Syndrome of renal magnesium wasting and nephrocalcinosis.

Authors:  R Lodha; P Hari; A Bagga
Journal:  Indian Pediatr       Date:  1999-10       Impact factor: 1.411

2.  Nephrocalcinosis in siblings--familial hypomagnesemia, hypercalciuria with nephrocalcinosis (FHHNC syndrome).

Authors:  M Ram Prabahar; R Manorajan; M E Fernando; R Venkatraman; V Balaraman; M Jayakumar
Journal:  J Assoc Physicians India       Date:  2006-06

3.  Familial Hypomagnesemia, Hypercalciuria and Nephrocalcinosis with Novel Mutation.

Authors:  S Margabandhu; M Doshi
Journal:  Indian J Nephrol       Date:  2019 Jan-Feb
  3 in total

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