Endocrinology

Trimethoprim–sulfamethoxazole-induced refractory hypoglycaemia successfully treated with octreotide
Jordan Kit Mah, Daniel Negreanu, Suhaib Radi, Stavroula Christopoulos

BMJ Case Reports CP May 2021, 14 (5) e240232; DOI: 10.1136/bcr-2020-240232
‘H-syndrome’: a multisystem genetic disorder with cutaneous clues
Krishna Shantilal Mori, Karthik Balachandran, Adyne Reena Asirvatham, Shriraam Mahadevan

BMJ Case Reports CP May 2021, 14 (5) e238973; DOI: 10.1136/bcr-2020-238973
Atypical presentation of autoimmune polyglandular syndrome type 1 in the fifth decade
Aditya Sanjeevi, Adlyne Reena Asirvatham, Karthik Balachandran, Shriraam Mahadevan

BMJ Case Reports CP Apr 2021, 14 (4) e241680; DOI: 10.1136/bcr-2021-241680
Development of central precocious puberty following cannabinoid use for paediatric epilepsy: causal or coincidence?
Aditya Krishnan, Juliana Chizo Agwu, Chetana Kallappa, Rajesh Pandey

BMJ Case Reports CP Apr 2021, 14 (4) e239678; DOI: 10.1136/bcr-2020-239678
Rare case of pancreatic neuroendocrine tumour presenting as paraneoplastic hypercalcaemia
Benjamin Ferrel, Jan Franko, May C Tee

BMJ Case Reports CP Apr 2021, 14 (4) e240786; DOI: 10.1136/bcr-2020-240786
Successful multidisciplinary treatment of Doege-Potter syndrome: hypoglycaemia caused by paraneoplastic IGF-2 production by a metastatic haemangiopericytoma
Jeffery Tong, Jonathan Athayde, Shawn MacKenzie, Meghan Ho

BMJ Case Reports CP Apr 2021, 14 (4) e241724; DOI: 10.1136/bcr-2021-241724
Perforated gastric ulcer as the initial manifestation of hyperparathyroidism
Cameron Castle, James Tietjens

BMJ Case Reports CP Apr 2021, 14 (4) e240570; DOI: 10.1136/bcr-2020-240570
Carney complex: a curious case of a rare cancer syndrome caused by a novel pathogenic mutation in the PRKAR1A gene
Nisha Gupta, Thomas Kitzler, Steffen Albrecht, Vincent Larouche

BMJ Case Reports CP Apr 2021, 14 (4) e241886; DOI: 10.1136/bcr-2021-241886
Perioperative management of cranial diabetes insipidus in a patient requiring a tracheostomy
Mairead Kelly, Misha Verkerk, Patrick Harrison, Richard Oakley

BMJ Case Reports CP Apr 2021, 14 (4) e239261; DOI: 10.1136/bcr-2020-239261
Focal congenital hyperinsulinism resulting from biallelic loss of function of KCNJ11 gene
Reema Garegrat, Suprabha Patnaik, Pradeep Suryawanshi, Chaitanya Datar

BMJ Case Reports CP Mar 2021, 14 (3) e240218; DOI: 10.1136/bcr-2020-240218

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Endocrinology

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