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Hereditary angioedema (HAE) is a genetic disorder that causes sudden episodes of swelling, often accompanied by abdominal pain. Affecting roughly 1 in 50 000 people, HAE typically appears in childhood ...
A woman in her 40s with a history of a subarachnoid haemorrhage complicated by ischaemic infarcts presented with 1 week of ...
Neurofibromatosis Type 1 (NF1) is a genetic disorder characterised by benign tumours and cutaneous lesions, including neurofibromas. This case report describes a boy in his early 10s with NF1 who ...
By definition, anteroposterior (AP) compression type 1 (APC-1) injury is a type of pelvic ring injury, which is widely acknowledged as ‘stable’. Unstable forms of this injury are very rare and present ...
We report a case of a woman in her 50s with chronic teprotumumab-associated sensorineural hearing loss. The patient presented with chronic thyroid eye disease with proptosis and diplopia despite ...
Figure 3 (A) H&E, 10×—mild to moderate spongiosis with dense perivascular and periadnexal infiltrate in the superficial and deep dermis. (B) H&E, 40×—the infiltrates consist mainly of neutrophils with ...
Transverse myelitis and cerebral venous thrombosis represent some of the described neurological complications of coronavirus disease. A woman in her early 30s presented with headache, left-sided ...
Laparoscopic segment 6 anatomical resection with utilisation of intraparenchymal indocyanine green (ICG) guidance for hepatocellular carcinoma (HCC) (30 June, 2025) ...
Spontaneous lens absorption and empty capsular bag in hyper-mature senile cataract (26 May, 2025 ...
We report a rare case of an early adolescent girl with Bartter syndrome presenting with severe vitamin A deficiency, characterised by decreased visual acuity, xerophthalmia and corneal ulceration. The ...
Congenital erythropoietic porphyria (CEP) also known as Gunther’s disease is a subtype of porphyria. It is an autosomal recessive disorder caused by a mutation in the uroporphyrinogen III gene (URO ...
Perianal Paget’s disease (PPD) is a rare condition which is often associated with underlying malignancy. To definitively rule ...