Oval window perilymph fistula in child with recurrent meningitis and unilateral hearing loss
10.1136/bcr-2020-234744
July 26, 2020
Paediatrics
CHARGE syndrome patient with novel CHD7 mutation presenting with severe laryngomalacia and feeding difficulty
10.1136/bcr-2019-233037
July 22, 2020
Child with Wyburn-Mason syndrome presenting with sudden onset of intracranial haemorrhage
10.1136/bcr-2020-237145
July 16, 2020
Simplified management of a giant forehead congenital nevus allows for early reconstruction
10.1136/bcr-2019-234164
July 13, 2020
Oral manifestations of lamellar ichthyosis in association with rickets
10.1136/bcr-2020-235008
July 8, 2020
Surgical downsizing of a prosthetic ring in congenital mitral valve regurgitation
10.1136/bcr-2020-235788
July 7, 2020
Laryngeal granular cell tumour: a very rare diagnosis for a child presenting with hoarse voice in the UK
10.1136/bcr-2019-232851
July 6, 2020
Progressive familial intrahepatic cholestasis type 4 in an Indian child: presentation, initial course and novel compound heterozygous mutation
10.1136/bcr-2019-234193
July 6, 2020
Two novel mutations in the CLCNKB gene leading to classic Bartter syndrome presenting as syncope and hypertension in a 13-year-old boy
10.1136/bcr-2019-233872
July 5, 2020
Congenital haemifacial hyperplasia
10.1136/bcr-2020-236504
July 5, 2020