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Results 1 - 10 of 11 for Thin corpus callosum
  1. Spastic paraplegia type 11 
    ... the condition. Autosomal recessive spastic paraplegia complicated with thin corpus callosum Autosomal recessive spastic paraplegia with mental impairment and ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-11 - Genetics
  2. Spastic paraplegia type 15 
    ... A. Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity. ... most common cause of hereditary spastic paraplegia with thin corpus callosum. Neurology. 2009 Oct 6;73(14):1111-9. ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  3. SPG11 gene 
    ... are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration. Brain. ... are a major cause of spastic paraplegia with thin corpus callosum. Nat Genet. 2007 Mar;39(3):366-72. ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  4. Chromosome 8 
    ... duplication 8p typically have severe intellectual disability, a thin or absent corpus callosum, weak muscle tone (hypotonia), abnormal curvature of the ...
    https://medlineplus.gov/genetics/chromosome/8 - Genetics
  5. Phosphoglycerate dehydrogenase deficiency 
    ... that connects the two halves of the brain (corpus callosum) is small and thin, and the fluid-filled cavities (ventricles) near the ...
    https://medlineplus.gov/...phosphoglycerate-dehydrogenase-deficiency - Genetics
  6. Xia-Gibbs syndrome 
    ... left and right halves of the brain (the corpus callosum) can be abnormally thin.Xia-Gibbs syndrome can also affect physical development. ...
    https://medlineplus.gov/genetics/condition/xia-gibbs-syndrome - Genetics
  7. Bohring-Opitz syndrome 
    ... left and right halves of the brain (the corpus callosum) can be abnormally thin.Eye problems that can affect vision also occur ...
    https://medlineplus.gov/genetics/condition/bohring-opitz-syndrome - Genetics
  8. FOXG1 syndrome 
    ... particular pattern of brain malformations that includes a thin or underdeveloped connection between the right and left halves of the brain (a structure called the corpus callosum), reduced folds and grooves (gyri) on the surface ...
    https://medlineplus.gov/genetics/condition/foxg1-syndrome - Genetics
  9. Absence of the Septum Pellucidum From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... is a rare neurological condition that involves the thin membrane located at the midline of the brain between the two cerebral hemispheres, or halves of the brain. It is connected to the corpus callosum -- a collection of nerve fibers that connect the ...
    https://www.ninds.nih.gov/.../disorders/absence-septum-pellucidum - External Health Links
  10. Opitz G/BBB syndrome 
    ... the left and right halves of the brain (corpus callosum). Distinct facial features that may be seen in this disorder include a prominent forehead, widow's peak hairline, flat nasal bridge, thin upper lip, and low-set ears. These features ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
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