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An interesting case of primary hypoparathyroidism

Primary hypoparathyroidism can occur due to an activating mutation of calcium sensing receptor (CaSR). Most patients remain asymptomatic and therefore not diagnosed until adulthood. We present a 38-year-old lady who had a history of muscle cramps since 8 years. She presented with vomiting, abdomen p...

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Autores principales: Kirpalani, D. A., Patel, J., Shah, H., Kirpalani, A., Amrapurkar, D., Choudhary, R., Dhurve, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127838/
https://www.ncbi.nlm.nih.gov/pubmed/25120296
http://dx.doi.org/10.4103/0971-4065.132018
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author Kirpalani, D. A.
Patel, J.
Shah, H.
Kirpalani, A.
Amrapurkar, D.
Choudhary, R.
Dhurve, A.
author_facet Kirpalani, D. A.
Patel, J.
Shah, H.
Kirpalani, A.
Amrapurkar, D.
Choudhary, R.
Dhurve, A.
author_sort Kirpalani, D. A.
collection PubMed
description Primary hypoparathyroidism can occur due to an activating mutation of calcium sensing receptor (CaSR). Most patients remain asymptomatic and therefore not diagnosed until adulthood. We present a 38-year-old lady who had a history of muscle cramps since 8 years. She presented with vomiting, abdomen pain and body ache, showed clinical evidence of hypovolemia, severe hypocalcemia, hypokalemia, hypomagnesemia, hyperphosphatemia and metabolic alkalosis. Her 24 h urinary phosphorus was low and 24 h urinary excretion of sodium, potassium and chloride were high. Her intact parathormone was on the lower side of the normal range. She improved once we had corrected her biochemical abnormalities. By excluding acquired causes of hypoparathyroidism, we are able to conclude that this may be a case of primary hypoparathyroidism due to activating mutation of CaSR.
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spelling pubmed-41278382014-08-12 An interesting case of primary hypoparathyroidism Kirpalani, D. A. Patel, J. Shah, H. Kirpalani, A. Amrapurkar, D. Choudhary, R. Dhurve, A. Indian J Nephrol Case Report Primary hypoparathyroidism can occur due to an activating mutation of calcium sensing receptor (CaSR). Most patients remain asymptomatic and therefore not diagnosed until adulthood. We present a 38-year-old lady who had a history of muscle cramps since 8 years. She presented with vomiting, abdomen pain and body ache, showed clinical evidence of hypovolemia, severe hypocalcemia, hypokalemia, hypomagnesemia, hyperphosphatemia and metabolic alkalosis. Her 24 h urinary phosphorus was low and 24 h urinary excretion of sodium, potassium and chloride were high. Her intact parathormone was on the lower side of the normal range. She improved once we had corrected her biochemical abnormalities. By excluding acquired causes of hypoparathyroidism, we are able to conclude that this may be a case of primary hypoparathyroidism due to activating mutation of CaSR. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4127838/ /pubmed/25120296 http://dx.doi.org/10.4103/0971-4065.132018 Text en Copyright: © Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kirpalani, D. A.
Patel, J.
Shah, H.
Kirpalani, A.
Amrapurkar, D.
Choudhary, R.
Dhurve, A.
An interesting case of primary hypoparathyroidism
title An interesting case of primary hypoparathyroidism
title_full An interesting case of primary hypoparathyroidism
title_fullStr An interesting case of primary hypoparathyroidism
title_full_unstemmed An interesting case of primary hypoparathyroidism
title_short An interesting case of primary hypoparathyroidism
title_sort interesting case of primary hypoparathyroidism
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127838/
https://www.ncbi.nlm.nih.gov/pubmed/25120296
http://dx.doi.org/10.4103/0971-4065.132018
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