Amy Mahood’s child MJ, who will be three next month, was diagnosed with 1p36 deletion syndrome when he was aged 14 months.

A BTK inhibitor combined with standard R-CHOP produced rapid, PET-defined complete remission in high-risk DLBCL-type Richter syndrome with TP53 deletion. Delaying ibrutinib until cycle 2 was used as a ...

Fifth-class students at St Matthew's National School, Ballymahon recently marked Rare Disease Awareness Day by showing solidarity and support for one their class-mates.

A 17-year-old boy with a rare condition has spent more than five months in hospital because there is no long-term care placement available for him.

Sidra Medicine, Qatar s specialist women s and children s hospital and a member of Qatar Foundation, has highlighted the real world ...

Most of you might measure Robert Horry’s impact through his clutch shots or his seven NBA championships, which he won during ...

Twelve-year-old Canberra girl Ashley Clifford and her family thought she was one of only two children in Australia with the very rare Beck-Fahrner syndrome. Your essential national news digest: all ...

To help children like Adley, you can donate to Arkansas Children’s Northwest’s “Champion for Children Giveathon” on the hospital’s website. This year’s theme is the “18 Challenge,” asking 18 people to ...

Jakob Tindle has a very rare condition called distil 5-Q deletion syndrome. The 17-year-old has been at Rotorua Hospital for more than five months - as he's become unpredictable and a danger to the ...

Sidra Medicine, a member of Qatar Foundation, has highlighted the real-world impact of precision medicine on a six-year-old patient with a rare genetic condition. Marking Rare Disease Day observed ...

Background and objective Most children with the rare disorder Silver-Russell syndrome (SRS) have feeding difficulties and/or gastrointestinal symptoms such as vomiting and constipation, worsening ...