Fluid electrolyte and acid-base disturbances

Hypokalaemic quadriparesis in a patient with urinary diversion through Indiana pouch
Srinivasa Anurag Kuchulakanti, Pradeep M Shenoy

BMJ Case Reports CP Apr 2022, 15 (4) e248123; DOI: 10.1136/bcr-2021-248123
Hyperglycinuria: diagnosis in middle age
Hithem Fargaly, Shobi Mathew, Noreen F Rossi

BMJ Case Reports CP Mar 2022, 15 (3) e246252; DOI: 10.1136/bcr-2021-246252
Use of Venous Excess UltraSound (VExUS) score in hyponatraemia management in critically ill patient
Rita Varudo, Inês Pimenta, Jacobo Bacariza Blanco, Filipe André Gonzalez

BMJ Case Reports CP Feb 2022, 15 (2) e246995; DOI: 10.1136/bcr-2021-246995
Successful living kidney donation from a patient with a Gitelman’s syndrome
Milad Darrat, Hannah Likinyo, Shin-Howe Ryan Winata, Sarah Morgan, Aisling E Courtney, John Lindsay

BMJ Case Reports CP Feb 2022, 15 (2) e246162; DOI: 10.1136/bcr-2021-246162
Refractory familial hypokalaemic periodic paralysis leading to cardiovascular compromise
Dominic O Awuah, Murtaza S Hussain, Anoosha Ponnapalli, Smit Sunil Deliwala, Elfateh M Seedahmed, Ghassan Bachuwa

BMJ Case Reports CP Feb 2022, 15 (2) e246674; DOI: 10.1136/bcr-2021-246674
Diagnostic and management considerations in pseudohypoaldosteronism type 1b
Jelte Kelchtermans, Sara E Pinney, Jacqueline M M Leonard, Sharon Mcgrath-Morrow

BMJ Case Reports CP Jan 2022, 15 (1) e246538; DOI: 10.1136/bcr-2021-246538
Topiramate-induced severe electrolyte abnormalities and hypernatremia leading to central pontine myelinolysis
Luba Muaddi, Omar Osman, Barbara Clark

BMJ Case Reports CP Nov 2021, 14 (11) e245870; DOI: 10.1136/bcr-2021-245870
Severe refeeding syndrome after human chorionic gonadotropin diet: a potentially lethal complication
Max J Schunemann, Martina Bertschinger, Christian Trachsel, Esther Bachli

BMJ Case Reports CP Nov 2021, 14 (11) e244011; DOI: 10.1136/bcr-2021-244011
MELAS syndrome: an acute stroke-like episode complicated by renal tubular acidosis
Dearbhail Ni Cathain, Emmet Browne, Kieran Skehan, Karl Boyle

BMJ Case Reports CP Nov 2021, 14 (11) e245898; DOI: 10.1136/bcr-2021-245898
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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