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  2. Cerebellar degeneration - Wikipedia

    en.wikipedia.org/wiki/Cerebellar_degeneration

    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 ]

  3. Neuroferritinopathy - Wikipedia

    en.wikipedia.org/wiki/Neuroferritinopathy

    Neuroferritinopathy is a genetic neurodegenerative disorder characterized by the accumulation of iron in the basal ganglia, cerebellum, and motor cortex of the human brain. . Symptoms, which are extrapyramidal in nature, progress slowly and generally do not become apparent until adulthood

  4. Anencephaly - Wikipedia

    en.wikipedia.org/wiki/Anencephaly

    Anencephaly is the absence of a major portion of the brain, skull, and scalp that occurs during embryonic development. [1] It is a cephalic disorder that results from a neural tube defect that occurs when the rostral (head) end of the neural tube fails to close, usually between the 23rd and 26th day following conception. [2]

  5. Pontocerebellar hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Pontocerebellar_hypoplasia

    Pontocerebellar hypoplasia (PCH) is a heterogeneous group of rare neurodegenerative disorders caused by genetic mutations and characterised by progressive atrophy of various parts of the brain such as the cerebellum or brainstem (particularly the pons). [1]

  6. Dandy–Walker malformation - Wikipedia

    en.wikipedia.org/wiki/Dandy–Walker_malformation

    Dandy–Walker malformation (DWM), also known as Dandy–Walker syndrome (DWS), is a rare congenital brain malformation in which the part joining the two hemispheres of the cerebellum (the cerebellar vermis) does not fully form, and the fourth ventricle and space behind the cerebellum (the posterior fossa) are enlarged with cerebrospinal fluid.

  7. CAPOS syndrome - Wikipedia

    en.wikipedia.org/wiki/CAPOS_syndrome

    Usually, individuals with this condition have cerebellar ataxia, areflexia, high-arched feet, optic nerve wasting/degeneration, sensorineural deafness. [5]These symptoms have variable onset, but they generally begin episodically after having a fever-causing infection such as the common cold, manifesting mainly as sudden-onset ataxic episodes and encephalopathy.

  8. Cerebellar hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Cerebellar_hypoplasia

    Cerebellar hypoplasia is characterized by reduced cerebellar volume, even though cerebellar shape is (near) normal. It consists of a heterogeneous group of disorders of cerebellar maldevelopment presenting as early-onset non–progressive congenital ataxia , hypotonia and motor learning disability .

  9. Birth defect - Wikipedia

    en.wikipedia.org/wiki/Birth_defect

    Fetal lymphocytes have been damaged as a result of a father's smoking habits prior to conception. [ 36 ] [ 38 ] Correlations between paternal smoking and the increased risk of offspring developing childhood cancers (including acute leukemia , brain tumors , and lymphoma ) before age five have been established.