The ratio of posterior wall thickness to the minimum voltage of QRS complexes in limb leads and several parameters derived from electrocardiography could independently predict ATTR-CM. The ratio of ...

Between 21.4% and 57.8% of patients from a real-world ATTR-CM cohort would have been eligible to take part in clinical trials testing disease-modifying therapies. Inclusion and exclusion criteria used ...

POEMS syndrome remains a diagnostic challenge due to its variable presentation and overlap with other demyelinating neuropathies, such as CIDP. Cases of polyneuropathy, organomegaly, endocrinopathy, ...

Diagnosis of neurofibromatosis type 1 (NF1) requires a combination of clinical assessment, genetic testing, and imaging studies. 1 NF1 is a rare genetic disorder characterized by the development of ...

Awareness of the key symptoms of NF1 can help in early diagnosis. A young male patient was diagnosed with neurofibromatosis type 1 (NF1) after undergoing detailed clinical investigations, according to ...

In all 6 CANVAS cases where SRAR was calculable, values exceeded 0.33 despite sometimes misleading length-dependent patterns. The sural/radial amplitude ratio (SRAR) as a valuable electrophysiological ...

Barriers to treatment include asparaginase toxicities, limited medical facilities and trained staff, and reduced care access and adherence. Issues of limited access to clinical trials and to expertise ...

The risk of iron overload in infants affected by Rh HDFN should be considered before prescribing iron supplementation. Neonates with hemolytic disease of the fetus and newborn (HDFN) due to Rhesus (Rh ...

Although a pregnant patient may exhibit a favorable response to IVIG treatment in one FNAIT-affected pregnancy, this does not ensure the success of IVIG therapy in subsequent pregnancies. A favorable ...

The AI ECG amyloid algorithm screening tool may provide decision support for clinicians and improve the diagnosis and survival of patients with ATTR-CM. A new study seeks to test an artificial ...

NMOSD is a rare autoimmune disorder characterized by inflammation and demyelination of nerves in the central nervous system (CNS), particularly the optic nerves and spinal cord. It typically manifests ...