Congenital sodium diarrhoea caused by rare de novo activating guanylate cyclase mutation
10.1136/bcr-2022-251632
December 29, 2022
Paediatrics
Spontaneous subdiaphragmatic bar migration after pectus excavatum treatment
10.1136/bcr-2022-251757
December 29, 2022
Growth hormone deficiency in a case of septo-optic-dysplasia due to SOX2 mutation: should we re-test patients during the transition period?
10.1136/bcr-2022-251897
December 29, 2022
Prenatal diagnosis and delivery of megalencephaly–capillary malformation syndrome
10.1136/bcr-2022-249587
December 26, 2022
Do renal and cardiac malformations in the fetus signal carnitine palmitoyltransferase II deficiency? A rare lethal fatty acid oxidation defect
10.1136/bcr-2022-251321
December 19, 2022
Diaphragmatic hernia: an infant in respiratory distress
10.1136/bcr-2022-252194
December 16, 2022
Cranial subdural migrating to lumbar subdural space in a toddler
10.1136/bcr-2022-251984
December 12, 2022
Use of tissue samples in diagnosing diploid triploid mosaicism
10.1136/bcr-2022-252779
December 8, 2022
Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant
10.1136/bcr-2022-248995
December 7, 2022
Anogenital condylomata acuminata in young children: not always result of sexual transmission
10.1136/bcr-2022-250591
December 5, 2022