ceroid-lipofuscinosis

ceroid-lipofuscinosis
neuronal ceroid-lipofuscinosis a term for several genetic lipidoses of diverse biochemical and clinical characteristics, all characterized by progressive neurodegeneration, loss of vision, and a fatal course; the infantile type is Haltia-Santavuori disease; the late infantile type is Jansky-Bielschowsky disease; the juvenile type is Vogt-Spielmeyer disease; and the adult type is Kufs disease.

Medical dictionary. 2011.

Игры ⚽ Поможем сделать НИР

Look at other dictionaries:

  • Neuronal ceroid lipofuscinosis — Classification and external resources ICD 10 E75.4 ICD 9 330.1 …   Wikipedia

  • lipofuscinosis — Abnormal storage of any one of a group of fatty pigments. ceroid l. SYN: Batten disease. neuronal ceroid l. a group of diseases characterized by accumulation of abnormal pigments in tissue (previously classified as …   Medical dictionary

  • Infantile neuronal ceroid lipfuscinosis — Infobox Disease Name = Infantile neuronal ceroid lipfuscinosis Caption = DiseasesDB = 31533 ICD10 = ICD9 = ICDO = OMIM = 256730 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D009472 INCL, also known as Infantile Neuronal Ceroid… …   Wikipedia

  • CLN — ceroid lipofuscinosis …   Medical dictionary

  • CLN — • ceroid lipofuscinosis …   Dictionary of medical acronyms & abbreviations

  • CLN5 — Ceroid lipofuscinosis, neuronal 5, also known as CLN5, is a human gene.cite web | title = Entrez Gene: CLN5 ceroid lipofuscinosis, neuronal 5| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1203| accessdate …   Wikipedia

  • CLN6 — Ceroid lipofuscinosis, neuronal 6, late infantile, variant, also known as CLN6, is a human gene.cite web | title = Entrez Gene: CLN6 ceroid lipofuscinosis, neuronal 6, late infantile, variant| url =… …   Wikipedia

  • CLN3 — Ceroid lipofuscinosis, neuronal 3 Identifiers Symbols CLN3; BTS; JNCL; MGC102840 External IDs …   Wikipedia

  • CLN8 — Ceroid lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation), also known as CLN8, is a human gene.cite web | title = Entrez Gene: CLN8 ceroid lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)| url =… …   Wikipedia

  • Lysosomale Speicherkrankheiten — (LSK) sind eine Gruppe von etwa 45 genetisch bedingten Stoffwechselerkrankungen, die durch Fehlfunktionen im Lysosom ausgelöst werden. Die Erkrankungen sind monogenetisch.[1] In der angelsächsischen Fachliteratur wird meist der Begriff Lysosomal… …   Deutsch Wikipedia

Share the article and excerpts

Direct link
… Do a right-click on the link above
and select “Copy Link”