Endocrinology

Ruptured functioning adrenal tumour, atypical presentation with renal colic and hypertension
Amr Elmoheen, Mohamed Yousry, Ahmed Elmesery, Khalid Bashir

BMJ Case Reports CP Dec 2020, 13 (12) e236050; DOI: 10.1136/bcr-2020-236050
Treatment-induced diabetes neuropathy: description of singular clinical signs to reach a prompt diagnosis
Pablo Guisado Vasco, Marcos Llanero-Luque, Marta Cano-Megías, María Cortés-Berdonces

BMJ Case Reports CP Dec 2020, 13 (12) e235165; DOI: 10.1136/bcr-2020-235165
Myasthenia gravis presenting as bilateral pseudointernuclear ophthalmoplegia in a patient with an incidental prolactinoma
Julian Fernando Arias Chavez, Cornelius James Fernandez

BMJ Case Reports CP Dec 2020, 13 (12) e234322; DOI: 10.1136/bcr-2020-234322
Oncogenic osteomalacia due to phosphaturic mesenchymal tumour in the upper thoracic spine
Bhavuk Garg, Nishank Mehta, Archit Goyal, Rajesh Khadgawat

BMJ Case Reports CP Dec 2020, 13 (12) e238209; DOI: 10.1136/bcr-2020-238209
Malignant prolongation of the QTc interval due to severe vitamin D deficiency: an unusual presentation
Preeti Gupta, Sourabh Agstam, Ashutosh Yadav, Soumitra Ghosh

BMJ Case Reports CP Dec 2020, 13 (12) e237157; DOI: 10.1136/bcr-2020-237157
Comprehensive evaluation of bone health using DXA and pQCT in an Indian boy with osteogenesis imperfecta
Madhura Bharat Karguppikar, Veena Ekbote, Anuradha Khadilkar, Vaman Khadilkar

BMJ Case Reports CP Dec 2020, 13 (12) e236169; DOI: 10.1136/bcr-2020-236169
Hyperandrogenism caused by ovarian Leydig cell tumour: finding the needle in a haystack
Chin Voon Tong, Yong Ting Tai

BMJ Case Reports CP Dec 2020, 13 (12) e238012; DOI: 10.1136/bcr-2020-238012
A Patient with speechlessness and rhabdomyolysis: a rare presentation of severe hypocalcaemia
Florine Helene Jiwa, Kim van den Hoek, Clementine Jaantje Joanna van Zeijl, Albertus Jozef Kooter

BMJ Case Reports CP Dec 2020, 13 (12) e238072; DOI: 10.1136/bcr-2020-238072
Diabetic thoracic radiculopathy: a case of a young woman with clinical improvement following immunotherapy
Alfonsa C Taiello, Vincenzo La Bella, Rossella Spataro

BMJ Case Reports CP Dec 2020, 13 (12) e236412; DOI: 10.1136/bcr-2020-236412
Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene
Willem M A Verhoeven, Jos I M Egger, Paddy K C Janssen, Arie van Haeringen

BMJ Case Reports CP Dec 2020, 13 (12) e235972; DOI: 10.1136/bcr-2020-235972

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Endocrinology

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