Children with cavernous malformations face unique treatment challenges due to factors such as the malformation's location, ...

Mitochondrial genome mutations may be linked to ALS, per a study, opening the door for new ways to diagnosing and treating ...

They share the same symptoms and are both caused by gene mutations. If you have one parent with familial hemiplegic migraine, you have a 50 percent of inheriting the condition. Sporadic hemiplegic ...

Almost all cases of ALS and half of frontotemporal dementia (FTD) cases are linked to dysfunction in a protein TDP-43.

RB mutations have been detected in retinoblastoma and a small fraction of sporadic tumors. RB is sequestered by viral oncoproteins, such as E1A, which prevent it from binding other factors.

It is rarely inherited, and is usually caused by sporadic dominant mutations. Cd LS displays many features commonly seen in isolation in sporadic birth defects, thus treatments developed for it may be ...

Intensifying mpox outbreak as both subclade Ia and Ib strains show signs of sustained human-to-human transmission in Kinshasa ...