Ehlers-Danlos syndromes (EDS) are a group of connective tissue disorders associated with skin, ligament, blood vessel and organ abnormalities. Skin hyperextensibility, joint hypermobility and widened ...
We present a male patient in his early 70s with a cyclical 20-year history of a nodular papule affecting the left forefoot. On examination, ginger red-coloured hairs were evident within the sinus ...
Rare cause of angina: mechanical compression from hydatid cyst (14 January, 2025) ...
We present a case of a woman in her 40s with disseminated enterovirus infection in the setting of maintenance therapy with ocrelizumab for relapsing-remitting multiple sclerosis. The patient ...
1 Department of Internal Medicine, University Sao Paulo State-UNESP, Botucatu, Sao Paulo, Brazil 2 Department of Internal Medicine, University Sao Paulo State, Botucatu, Sao Paulo, Brazil Acute kidney ...
Primary bone lymphoma is a rare type of lymphoma that arises from skeletal tissue. Most cases described are non-Hodgkin’s lymphoma with diffuse large B-cell lymphoma being the most common subtype.
Doxycycline is a commonly prescribed antibiotic with growing evidence suggesting a possible linkage with drug-induced acute pancreatitis. We present an elderly female presenting with severe acute ...
Craniorachischisis totalis (anencephaly with total open spina bifida) is the most severe form of neural tube defects. The exact aetiology of neural tube defects remains poorly understood. We report a ...
Complications of stroke can include neuropsychiatric symptoms. However, post-stroke psychosis is rare. We report a case where an acute presentation of psychosis, depression and fluctuating cognitive ...
True isolated sixth nerve palsy as the initial presentation of multiple sclerosis (MS) is rare. MS is a chronic inflammatory, immune-mediated disease of the central nervous system. This is the most ...
1 Department of Obstetrics and Gynaecology, St Mary's Hospital, London, UK 2 Department of Obstetrics and Gynaecology, Princess of Wales Hospital, Wales, UK 3 Department of Obstetrics and Gynaecology, ...
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive ciliopathy characterised by rod-cone dystrophy, obesity, postaxial polydactyly, cognitive impairment, hypogonadism, renal abnormalities, and ...