familial encephalopathy

См. также в других словарях:

• Familial encephalopathy with neuroserpin inclusion bodies — Classification and external resources OMIM 604218 Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a progressive disorder of the nervous system that is characterized by a loss of intellectual functioning (dementia) and… …   Wikipedia

• Encephalopathy — Classification and external resources ICD 9 348.30 MeSH D001927 Encephalopathy /ɛnˌsɛfəˈlɒpəθi/ means disorder or disease …   Wikipedia

• Transmissible spongiform encephalopathy — Transmissible spongiform encephalopathies (TSEs, also known as prion diseases) are a group of progressive conditions that affect the brain and nervous system of animals. According to the most widespread hypothesis they are transmitted by prions,… …   Wikipedia

• Hepatic encephalopathy — Classification and external resources Micrograph of Alzheimer type II astrocytes, as may be seen in hepatic encephalopathy. ICD 10 …   Wikipedia

• Fatal familial insomnia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 32177 ICD10 = ICD10|A|81|9|a|80 ICD9 = ICD9|046.8 ICDO = OMIM = 600072 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D034062 Fatal familial insomnia (FFI) is a very rare autosomal… …   Wikipedia

• fatal familial insomnia — an autosomal dominant disorder due to a mutation in the gene for the prion protein (PrP): it is an example of a spongiform encephalopathy. Patients present with intractable progressive insomnia, disturbances of the autonomic nervous system, and… …   Medical dictionary

• fatal familial insomnia — an autosomal dominant disorder due to a mutation in the gene for the prion protein (PrP): it is an example of a spongiform encephalopathy. Patients present with intractable progressive insomnia, disturbances of the autonomic nervous system, and… …   The new mediacal dictionary

• Neurodegeneration — Classification and external resources Para sagittal MRI of the head in a patient with benign familial macrocephaly. ICD 10 G30 G32 …   Wikipedia

• SERPINI1 — Serpin peptidase inhibitor, clade I (neuroserpin), member 1 PDB rendering based on 1jjo …   Wikipedia

• Serpin — Serpins are a group of proteins with similar structures that were first identified as a set of proteins able to inhibit proteases. The name serpin is derived from this activity serine protease inhibitors. [cite journal |author=R. Carrell and J.… …   Wikipedia

• Aicardi-Goutieres syndrome — Infobox Disease Name = Aicardi Goutieres syndrome Caption = DiseasesDB = 31680 ICD10 = ICD9 = ICDO = OMIM = 225750 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Aicardi Goutieres syndrome is a rare genetic disorder. It is also known as… …   Wikipedia