WebBulbar palsy refers to a set of signs and symptoms linked to the impaired function of the lower cranial nerves, typically caused by damage to their lower motor neurons or to the lower cranial nerve itself. The impacted cranial nerves are a set of nerves that arise straight from the brainstem and include cranial nerves IX (9), X (10), XI (11 ... WebJan 28, 2024 · Changes in a gene called PRNP that makes prion protein cause the genetic forms of the disease. Rare genetic forms also include Gerstmann-Straussler-Scheinker syndrome. This syndrome causes …
Rett syndrome - Symptoms and causes - Mayo Clinic
WebMuscular dystrophy is a group of inherited diseases characterized by weakness and wasting away of muscle tissue, with or without the breakdown of nerve tissue. There are 9 types of muscular dystrophy, … WebDec 24, 2024 · People with multiple sclerosis may also develop: Muscle stiffness or spasms. Severe weakness or paralysis, typically in the legs. Problems with bladder, bowel or sexual function. Cognitive problems, … godfather iii quote they pull me back in
Ehlers-Danlos syndrome - Symptoms and causes - Mayo Clinic
WebMar 17, 2011 · What Do We Know About Heredity and Tay-Sachs Disease? Tay-Sachs disease (TSD) is a fatal genetic disorder, most commonly occurring in children, that results in progressive destruction of the … WebPeople with hereditary cerebral amyloid angiopathy often have progressive loss of intellectual function (dementia), stroke, and other neurological problems starting in mid … Fatal familial insomnia is a rare hereditary prion disease that is associated with the D178N-129M PRNP gene that is caused by a mutation. The gene PRNP that provides instructions for making the prion protein PrP is located on the short (p) arm of chromosome 20 at position p13. Both people with FFI and those with familial Creutzfeldt–Jakob disease (fCJD) carry a mutation at codon 178 of the … bonus gestione separata inps