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  • Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation

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Endocrinology
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation

Authors

  • Savita Khadse Pediatrics, Lokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College, Mumbai, Maharashtra, India PubMed articlesGoogle scholar articles
  • Vrushali Satish Takalikar Pediatrics, Lokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College, Mumbai, Maharashtra, India PubMed articlesGoogle scholar articles
  • Radha Ghildiyal Pediatrics, Lokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College, Mumbai, Maharashtra, India PubMed articlesGoogle scholar articles
  • Nikhil Shah Pediatrics, Lokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College, Mumbai, Maharashtra, IndiaDivision Of Pediatric Endocrinology, Department of Pediatrics, Surya Children's Hospital, Mumbai, India PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Nikhil Shah; nikhilshah1507{at}gmail.com
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Citation

Khadse S, Takalikar VS, Ghildiyal R, et al
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation
BMJ Case Reports CP 2024;17:e257505.

Publication history

  • Accepted February 15, 2024
  • First published February 26, 2024.
Online issue publication 
February 26, 2024

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