Idiopathic hypogonadotropic hypogonadism: a rare cause of primary amenorrhoea in adolescence—a review and update on diagnosis, management and advances in genetic understanding.
10.1136/bcr-2020-239495
April 9, 2021
Paediatrics
PIEZO1 mutation: a rare aetiology for fetal ascites
10.1136/bcr-2020-240682
April 9, 2021
Maternal finger-prick allogenic blood for persistent corneal epithelial defects
10.1136/bcr-2020-241138
April 9, 2021
Type 3 antenatal Bartter syndrome presenting with mild polyuria
10.1136/bcr-2021-242086
April 7, 2021
Vaginal bleeding in a misdiagnosed Mayer-Rokitansky-Küster-Hauser syndrome
10.1136/bcr-2020-241387
April 5, 2021
Tracheal cartilaginous sleeve in Pfeiffer syndrome: lesson learnt from its rarity
10.1136/bcr-2020-236888
April 2, 2021
Brain-lung-thyroid syndrome in a neonate with argininosuccinate lyase deficiency
10.1136/bcr-2020-241032
March 31, 2021
Reducing suspicion of sexual abuse in paediatric chlamydial conjunctivitis using ompA genotyping
10.1136/bcr-2020-238871
March 29, 2021
Bilobed tongue base associated with multiple branchial anomalies
10.1136/bcr-2020-241081
March 29, 2021
Acute haemorrhagic oedema of infancy as a manifestation of COVID-19
10.1136/bcr-2020-241111
March 29, 2021