A new study conducted in India has revealed that 40% of antenatal patients experienced severe fetomaternal hemorrhage, which can increase the risk of HDFN.

Large language models may offer complementary value to human expert analysis in the diagnosis of achondroplasia and other skeletal dysplasias.

Frailty reduced the likelihood of CLL/SLL first-line treatment initiation during the CIT era, but the gap narrowed with novel therapies.

Compound 23, a dual-target FGFR2/3 inhibitor, delivered superior growth improvements over infigratinib in achondroplasia mouse models.

Biomarkers are increasingly recognized for their use in diagnosing and tracking disability progression in NMOSD.

Long-term prophylaxis with lanadelumab has been linked to a marked reduction in attack rates in HAE, with the decline persisting in a real-world setting.

TTR amyloid deposition was present in the vessel walls of different organs throughout the body in ATTR-CM and Alzheimer’s disease, a study found.

There was high consensus among neurologists on treating acute attacks with high-dose steroids and plasmapheresis in severe cases. Rituximab is still the most prescribed treatment for neuromyelitis ...

Forskolin may help increase the regeneration of the muscle tissue and reduce fibrosis in Duchenne muscular dystrophy (DMD), a study found.

Total joint arthroplasty may be a safe and durable treatment option for patients with achondroplasia, a form of skeletal dysplasia.

The prevalence of PBC is expected to rise in the United States and the wider world, requiring concrete, proactive action.

Fostamatinib has been found to be safe and effective in patients with heavily treated persistent/chronic immune thrombocytopenia (ITP).