Search results
Results from the WOW.Com Content Network
Cerebellar degeneration is a condition in which cerebellar cells, otherwise known as neurons, become damaged and progressively weaken in the cerebellum. [1] There are two types of cerebellar degeneration; paraneoplastic cerebellar degeneration , and alcoholic or nutritional cerebellar degeneration. [ 2 ]
334.2 Primary cerebellar degeneration; 334.3 Other cerebellar ataxia; 334.4* Cerebellar ataxia in diseases classified elsewhere; 334.8 Other; 334.9 Unspecified; 335 Anterior horn cell disease. 335.0 Werdnig-Hoffmann disease; 335.1 Spinal muscular atrophy; 335.2 Motor neurone disease; 335.8 Other; 335.9 Unspecified; 336 Other diseases of spinal cord
Download QR code; Print/export Download as PDF; Printable version; In other projects ... MeSH C10.228.140.252.620 – paraneoplastic cerebellar degeneration;
Paraneoplastic cerebellar degeneration (PCD) is a paraneoplastic syndrome associated with a broad variety of tumors including lung cancer, ovarian cancer, breast cancer, Hodgkin’s lymphoma and others. PCD is a rare condition that occurs in less than 1% of cancer patients.
Ramsay Hunt syndrome type 1, also called Ramsay Hunt cerebellar syndrome, is a rare form of cerebellar degeneration which involves myoclonic epilepsy, progressive ataxia, tremor, and a dementing process. [1] Ramsay Hunt syndrome type 2 is the reactivation of herpes zoster in the geniculate ganglion.
12585 Ensembl ENSG00000140743 ENSMUSG00000030878 UniProt Q01850 P97817 RefSeq (mRNA) NM_001802 NM_007672 NM_001354986 RefSeq (protein) NP_001793 NP_031698 NP_001341915 Location (UCSC) Chr 16: 22.35 – 22.44 Mb Chr 7: 120.56 – 120.58 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Cerebellar degeneration-related protein 2 is a protein that in humans is encoded by the CDR2 gene. See ...
Codes following these are found at List of MeSH codes ... MeSH C23.550.737.750 – wallerian degeneration; ... MeSH C23.888.592.350.090.200 – cerebellar ataxia;
Babies with this condition usually appear normal at birth, but start showing symptoms when they are just 6 months old, these symptoms are (but are not limited to): hypotonia, developmental delays, seizures, bobbing of the head, abnormal twitching and movement of the muscles, and loss of braincells from the cerebellum, retinal degeneration, involuntary rapid movement of the eyes, and strabismus.