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      Complexities surrounding the diagnosis and management of hypercalcaemia in pregnancy

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          Abstract

          Summary

          Hypercalcaemia in pregnancy is uncommon, with associated adverse obstetric and perinatal outcomes for both the mother and the fetus. Determination of causality is central to its management. Diagnostic imaging techniques are limited during pregnancy and the diagnosis is made more complex by physiological changes in calcium and vitamin D homeostasis in pregnancy. Further, therapeutic options are limited due to safety considerations for the pregnant woman and the developing foetus. Three cases of hypercalcaemia in pregnancy will be presented, highlighting the distinct aetiologies and management strategies for hypercalcaemia in pregnancy and the importance of early measurement of serum calcium in pregnancy screening.

          Learning points
          • There are complex physiological changes in calcium balance in pregnancy, including increased calcium intestinal absorption and renal excretion.

          • Hypercalcaemia in pregnancy is uncommon but has important potential maternal and foetal complications, making a compelling argument for routine antenatal, calcium screening.

          • Identifying the cause of hypercalcaemia in pregnancy can be challenging due to the complex placental interplay in biochemical test interpretation and due to safety constraints restricting imaging and surgery.

          • Acute medical management of hypercalcaemia must be considered in the context of both maternal and foetal well-being, along with gestational age and specific consideration for the safety of the developing fetus in late gestation.

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          Most cited references10

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          Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.

          The calcium-sensing receptor (CASR) is a plasma membrane G protein coupled receptor that is expressed in the parathyroid hormone (PTH) producing chief cells of the parathyroid gland and the cells lining the kidney tubule. By virtue of its ability to sense small changes in circulating calcium concentration ([Ca(2+)](o)) and to couple this information to intracellular signaling pathways that modify PTH secretion or renal cation handling, the CASR plays an essential role in maintaining mineral ion homeostasis. Inherited abnormalities of the CASR gene located on chromosome 3p13.3-21 can cause either hypercalcemia or hypocalcemia depending upon whether they are inactivating or activating, respectively. Heterozygous loss-of-function mutations give rise to familial (benign) hypocalciuric hypercalcemia (FHH) in which the lifelong hypercalcemia is asymptomatic. The homozygous condition manifests itself as neonatal severe hyperparathyroidism (NSHPT), a rare disorder characterized by extreme hypercalcemia and the bony changes of hyperparathyroidism which occur in infancy. The disorder autosomal dominant hypocalcemia (ADH) is due to gain-of-function mutations in the CASR gene. ADH may be asymptomatic or present with neonatal or childhood seizures. A common polymorphism in the intracellular tail of the CASR, Ala to Ser at position 986, has a modest effect on the serum calcium concentration in healthy individuals. Copyright 2000 Wiley-Liss, Inc.
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            Pregnancy outcomes in women with primary hyperparathyroidism.

            Primary hyperparathyroidism (PHPT) during pregnancy may pose considerable risks to mother and fetus. This study examined pregnancy outcomes in women with gestational PHPT in relation to clinical and laboratory parameters.
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              Maternal-fetal calcium and bone metabolism during pregnancy, puerperium, and lactation.

                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                EDM
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                20 April 2021
                2021
                : 2021
                : 20-0163
                Affiliations
                [1 ]Department of Diabetes and Endocrinology , Royal North Shore Hospital, Sydney, Australia
                [2 ]Northern Clinical School , Department of Medicine, University of Sydney, Australia
                [3 ]Kolling Institute of Medical Research , Royal North Shore Hospital, Sydney, Australia
                Author notes
                Correspondence should be addressed to N Rodrigo; Email: natassia.rodrigo@ 123456sydney.edu.au
                Article
                EDM200163
                10.1530/EDM-20-0163
                8185537
                33982664
                c45f582c-1b53-400d-93c0-22df18b512ff
                >© The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License..

                History
                : 25 March 2021
                : 20 April 2021
                Categories
                Pregnant Adult
                Female
                White
                Australia
                Parathyroid
                Bone
                Obstetrics
                Unique/Unexpected Symptoms or Presentations of a Disease
                Unique/Unexpected Symptoms or Presentations of a Disease

                pregnant adult,female,white,australia,parathyroid,bone,obstetrics,unique/unexpected symptoms or presentations of a disease,may,2021

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