Rare disease

Coatomer-associated protein subunit alpha syndrome: abnormal trafficking between the Golgi complex and the endoplasmic reticulum
Julie Perrin, Nicolas Roux, François Maurier

BMJ Case Reports CP Nov 2020, 13 (11) e231553; DOI: 10.1136/bcr-2019-231553
Subretinal abscess as an initial presentation of systemic nocardiosis
Muhammad Bilal Malik, Nida Jawed Ahsan, Kiran Hilal, Syed Faisal Mahmood, M A Rehman Siddiqui

BMJ Case Reports CP Nov 2020, 13 (11) e236898; DOI: 10.1136/bcr-2020-236898
Rare pulmonary embolism caused by the combination of bilateral popliteal venous aneurysms and antiphospholipid syndrome
Tomoki Fukui, Nobuyuki Ogasawara, Shinji Hasegawa

BMJ Case Reports CP Nov 2020, 13 (11) e236341; DOI: 10.1136/bcr-2020-236341
Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome
Ebner Bon Gatus Maceda, Lisa E Kratz, Veronica Marie E Ramos, Mary Ann R Abacan

BMJ Case Reports CP Nov 2020, 13 (11) e236859; DOI: 10.1136/bcr-2020-236859
Mephentermine dependence in a young Indian adult without psychosis
Aditya Somani

BMJ Case Reports CP Nov 2020, 13 (11) e236924; DOI: 10.1136/bcr-2020-236924
Oesophageal lung: a rare cause of complete hemithorax opacification
Padma Vikram Badhe, Abhishek Bairy, Karthik Shivappa Huruli

BMJ Case Reports CP Nov 2020, 13 (11) e234539; DOI: 10.1136/bcr-2020-234539
Squamous cell carcinoma of the rectum
Deep Chakrabarti, Sumaira Qayoom, Naseem Akhtar, Rajeev Gupta

BMJ Case Reports CP Oct 2020, 13 (10) e236256; DOI: 10.1136/bcr-2020-236256
Oesophageal GIST
Filipa Costa, Rui Casaca, Cecilia Monteiro, Paulo Ramos

BMJ Case Reports CP Oct 2020, 13 (10) e238058; DOI: 10.1136/bcr-2020-238058
Maternal complications of fetal triploidy: a case report
Sarah Wali, Marianne Wild

BMJ Case Reports CP Oct 2020, 13 (10) e236950; DOI: 10.1136/bcr-2020-236950
Rare cause of right iliac fossa pain in a UK patient
Khurram Shahzad, Mohamed Elmedani, Smitha Mathew, Ioannis Peristerakis

BMJ Case Reports CP Oct 2020, 13 (10) e234694; DOI: 10.1136/bcr-2020-234694

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Rare disease

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