Uncommon presentation: monozygotic twins with Turner syndromeBushra Rehman, Yumna Shariff, Muzna Arif, Fozia Memon
30 October 2024
Neonatal respiratory distress syndrome in E292V homozygous ABCA3Anne Stone, Trang Huynh
30 October 2024
Eye movement desensitisation and reprocessing (EMDR) therapy in preterm children with selective mutismCoby Mesman, Iris Van Der Horst, Fien Spijker-Verkerk, Jan Erik Bunt
24 October 2024
Subtle echocardiogram findings requiring further investigation: restrictive cardiomyopathy in a rare genetic conditionJudah Andrew Kreinbrook, Laura Izzo, Christopher Atkins, Samrat Das
23 October 2024
Polyarteritis nodosa mimics Kawasaki diseaseIbrahim Alibrahim, Aisha Mirza, Amer Khojah
21 October 2024
Congenital saccular cyst of the larynx: a rare cause of stridor in a newborn infantSanjna Nilesh Nerurkar, Shrenik Vora, Huiting Lynn Koh, Suresh Chandran
18 October 2024
Collapse of an early adolescent girl. Syncope? Simple or sinister?Graham Martin, Chiara Cavaliere, Nikila Pandya, Krishnan Balasubramanian
15 October 2024
Neonatal hyperekplexia: a non-epileptic paroxysmal movement disorder with a novel homozygous mutation in the GLRB gene, a seizure mimicHera Fatima, Shabnam Shabnam, Shalini Tripathi, Mala Kumar
15 October 2024
Hand, foot and mouth disease-induced onychomadesisTomotaka Takanosu
14 October 2024
Novel cause of bilateral proptosis in a child: orbital extramedullary haematopoietic tissue due to iron deficiency anaemiaAbhijeet Vilas Botre, Sarita Verma, Ambrishkumar Dayashankar Mishra
14 October 2024