• Cerebellar hypoplasia (CH) is a neurological condition in which the cerebellum is smaller than usual or not completely developed. It has been reported...
    13 KB (1,272 words) - 09:49, 13 August 2024
  • Thumbnail for Cerebellar hypoplasia
    Cerebellar hypoplasia is characterized by reduced cerebellar volume, even though cerebellar shape is (near) normal. It consists of a heterogeneous group...
    9 KB (905 words) - 11:29, 24 June 2024
  • deficiency present at birth Cerebellar hypoplasia, characterized by reduced cerebellar volume Cerebellar hypoplasia (non-human) French catheter scale (Charrière)...
    4 KB (459 words) - 19:36, 6 November 2024
  • urination or defecation. Cats portal Canine cognitive dysfunction Cerebellar hypoplasia (non-human) Feline spongiform encephalopathy Ilona Rodan; Sarah Heath...
    9 KB (962 words) - 02:46, 31 July 2024
  • Thumbnail for Cerebellum
    Cerebellum (redirect from Cerebellar nuclei)
    in humans with Gorlin Syndrome and in genetically engineered mouse models. Congenital malformation or underdevelopment (hypoplasia) of the cerebellar vermis...
    95 KB (11,629 words) - 19:34, 30 October 2024
  • regardless of etiology. Causes of CCAS include cerebellar agenesis, dysplasia and hypoplasia, cerebellar stroke, tumor, cerebellitis, trauma, and neurodegenerative...
    27 KB (3,192 words) - 18:40, 17 August 2024
  • Thumbnail for Cerebellar abiotrophy
    Cerebellar abiotrophy in horses was originally thought to be a form of cerebellar hypoplasia (CH) and was described as such in older research literature. However...
    23 KB (2,484 words) - 17:01, 23 September 2024
  • affected people have a form of non-progressive congenital cerebellar ataxia. The brain impairments include cerebellar hypoplasia, mild cerebral cortex atrophy...
    5 KB (536 words) - 15:13, 7 September 2024
  • Thumbnail for Dandy–Walker malformation
    terms or criteria should be used. The core criteria of DWM are hypoplasia of the cerebellar vermis and an enlarged fourth ventricle and posterior fossa (the...
    47 KB (5,483 words) - 15:13, 2 March 2024
  • Thumbnail for Aniridia
    development, but is a panocular condition with macular and optic nerve hypoplasia, cataract, and corneal changes. Vision may be severely compromised and...
    9 KB (901 words) - 14:22, 29 August 2024
  • Thumbnail for Purkinje cell
    inability to determine space and distance. A similar condition known as cerebellar hypoplasia occurs when Purkinje cells fail to develop in utero or die off before...
    29 KB (3,300 words) - 01:00, 1 November 2024
  • Thumbnail for VLDL receptor
    VLDL receptor (category Genes on human chromosome 9)
    variety of symptoms and diseases, which include type I lissencephaly, cerebellar hypoplasia, and atherosclerosis. VLDLR is a member of the low-density-lipoprotein...
    37 KB (4,708 words) - 03:20, 26 October 2023
  • Thumbnail for Chiari malformation
    the cerebellum, characterized by a downward displacement of one or both cerebellar tonsils through the foramen magnum (the opening at the base of the skull)...
    52 KB (4,861 words) - 11:07, 22 October 2024
  • Thumbnail for Mental retardation and microcephaly with pontine and cerebellar hypoplasia
    Mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH) – also known as mental retardation, X-linked, syndromic, Najm type...
    19 KB (2,043 words) - 02:42, 13 July 2024
  • Thumbnail for OPHN1
    OPHN1 (category Genes on human chromosome X)
    associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia". European Journal of Human Genetics. 7 (5): 541–8. doi:10.1038/sj.ejhg...
    10 KB (1,188 words) - 00:29, 3 December 2023
  • Thumbnail for 3C syndrome
    syndrome is a rare condition whose symptoms include heart defects, cerebellar hypoplasia, and cranial dysmorphism. It was first described in the medical...
    13 KB (1,320 words) - 12:38, 20 October 2024
  • Thumbnail for Nystagmus
    abscess (cerebellar) Cerebellar ataxia Chiari malformation Multiple sclerosis Stroke Thalamic hemorrhage Trauma Tumor Infantile cerebellar retinal degeneration...
    37 KB (4,090 words) - 12:43, 1 November 2024
  • Thumbnail for Cerebral palsy
    PMID 25981959. Case 6 had cerebellar vermis hypoplasia and Case 7 had global cerebellar hypoplasia (vermis and cerebellar hemispheres), both these cases...
    171 KB (19,227 words) - 09:27, 9 November 2024
  • Thumbnail for Canine parvovirus
    pups can be born with neurological abnormalities such as cerebellar hypoplasia. CPV2 is a non-enveloped single-stranded DNA virus in the Parvoviridae family...
    30 KB (3,496 words) - 19:23, 22 November 2024
  • Thumbnail for Ciliopathy
    Breathing abnormalities Cerebellar vermis hypoplasia Diabetes Exencephaly Eye movement abnormalities Hydrocephalus Hypoplasia of the corpus callosum Hypotonia...
    35 KB (2,499 words) - 18:40, 12 July 2024
  • Thumbnail for Strømme syndrome
    in zebrafish whose CENPF genes were experimentally knocked out. Cerebellar hypoplasia in association with hydrocephalus can constitute Dandy–Walker malformation...
    25 KB (2,717 words) - 18:28, 25 March 2024
  • Thumbnail for Cat health
    impaction Cerebellar hypoplasia is a disorder found in cats and dogs in which the cerebellum is not completely mature at birth. Cerebellar hypoplasia causes...
    31 KB (3,352 words) - 09:51, 4 September 2024
  • Thumbnail for Goldberg–Shprintzen syndrome
    D'Alonzo, Gabriella; Papalia, Francesco (2003-05-01). "Pachygyria and cerebellar hypoplasia in Goldberg-Shprintzen syndrome". American Journal of Medical Genetics...
    13 KB (1,326 words) - 23:08, 23 October 2024
  • Thumbnail for Chudley–Mccullough syndrome
    consanguineous Lebanese parents, with infancy-onset hearing loss, hypoplasia of the inferior cerebellar vermis and corpus callosum, frontal parasagittal polymicrogyria...
    13 KB (1,346 words) - 01:05, 24 June 2024
  • Thumbnail for Chromosome 9
    purpura trisomy 9 tuberous sclerosis VLDLR-associated cerebellar hypoplasia G-banding ideograms of human chromosome 9 "Search results - 1[CHR] AND "Homo sapiens"[Organism]...
    26 KB (1,594 words) - 20:53, 24 August 2024
  • Thumbnail for Proto-oncogene Wnt-1
    Proto-oncogene Wnt-1 (category Genes on human chromosome 12)
    gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the...
    9 KB (1,008 words) - 17:50, 10 April 2024
  • Thumbnail for Lissencephaly
    (September 2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–6. doi:10...
    24 KB (2,534 words) - 20:22, 31 October 2024
  • Thumbnail for Cowden syndrome
    disability have been reported as well. Lhermitte-Duclos disease is a benign cerebellar tumor that typically does not manifest until adulthood in patients with...
    23 KB (2,139 words) - 22:37, 10 June 2024
  • Thumbnail for Mumps
    complications of infection include: paralysis, seizures, cranial nerve palsies, cerebellar ataxia, transverse myelitis, ascending polyradiculitis, a polio-like disease...
    63 KB (7,827 words) - 21:57, 18 October 2024
  • Thumbnail for Veterinary virology
    any age, leading to vomiting, diarrhea and immunosuppression but cerebellar hypoplasia is only seen in cats that were infected in the womb or at less than...
    12 KB (1,386 words) - 05:20, 8 February 2024