Fluid electrolyte and acid-base disturbances

Atypical haemolytic uremic syndrome from multiple missenses to a full-blown disease
Filipe Santos Mira, Ana Luísa Nunes, Ana Rita Elvas, Nuno Oliveira

BMJ Case Reports CP Jun 2019, 12 (6) e230026; DOI: 10.1136/bcr-2019-230026
Partial nephrogenic diabetes insipidus associated with lithium therapy
Eka Nandoshvili, Steve Hyer, Nikhil Johri

BMJ Case Reports CP Sep 2019, 12 (9) e231093; DOI: 10.1136/bcr-2019-231093
Rare brown tumour of the mandible secondary to tertiary hyperparathyroidism in a renal transplant recipient
Aurélien M Guéroult, Malcolm Cameron

BMJ Case Reports CP Sep 2019, 12 (9) e231231; DOI: 10.1136/bcr-2019-231231
Hypercalcaemia due to isolated elevation of 1,25-dihydroxyvitamin D in patients with Crohn’s disease
Faisal Inayat, Saad Saleem, Adil Mohyudin, Zubair Khan

BMJ Case Reports CP Sep 2019, 12 (9) e230099; DOI: 10.1136/bcr-2019-230099
Cyclical haematological changes in a case of hypopituitarism
Rahul Nema, Abhinav Sengupta, Arvind Kumar, Naveet Wig

BMJ Case Reports CP Aug 2021, 14 (8) e243421; DOI: 10.1136/bcr-2021-243421
Severe metabolic derangement: a case of concomitant diabetic ketoacidosis and beer potomania
Dmitriy Stasishin, Patrick Schaffer, Zeryab Khan, Christie Murphy

BMJ Case Reports CP Aug 2021, 14 (8) e243486; DOI: 10.1136/bcr-2021-243486
Pituitary microadenoma with hypopituitarism presenting as hyponatremia
Robin George Manappallil, Pradeep Puthen Veetil, Harish Babu, Sadab Raza Khan

BMJ Case Reports CP Aug 2021, 14 (8) e244426; DOI: 10.1136/bcr-2021-244426
Management of hyponatraemia in pre-eclampsia with severe features
Julia Whitley, Sarah Swartz, Anjali Martinez

BMJ Case Reports CP Aug 2021, 14 (8) e244688; DOI: 10.1136/bcr-2021-244688
Refractory hypokalaemia and hypertension with metabolic alkalosis: an acute presentation of Cushing’s disease secondary to a pituitary macroadenoma
Najeeb Zaheer Shah, Shah Malik, Thozhukat Sathyapalan, Kamrudeen Mohammed

BMJ Case Reports CP Aug 2021, 14 (8) e244850; DOI: 10.1136/bcr-2021-244850
Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene
Srinivasan Mani, Jayasree Nair, Deepali Handa

BMJ Case Reports CP Oct 2021, 14 (10) e244685; DOI: 10.1136/bcr-2021-244685

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Fluid electrolyte and acid-base disturbances

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