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Results 11 - 20 of 58 for Cerebral white matter hypoplasia
  1. Megalencephalic leukoencephalopathy with subcortical cysts 
    ... head (macrocephaly). Affected people also have leukoencephalopathy, an abnormality of the brain's white matter. White matter consists of nerve fibers covered by ...
    https://medlineplus.gov/...eukoencephalopathy-with-subcortical-cysts - Genetics
  2. Combined oxidative phosphorylation deficiency 1 
    ... the two halves of the brain (corpus callosum hypoplasia) and loss of brain tissue called white matter (leukodystrophy), particularly in an area of the brain ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  3. Congenital fibrosis of the extraocular muscles 
    ... neuropathy), which can begin in childhood or adulthood.Brain abnormalities can also occur in people with CFEOM3. Some have abnormal development of the white matter, which is brain tissue containing nerve cell fibers ( ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics
  4. D-bifunctional protein deficiency 
    ... in the brain and spinal cord; loss of white matter is described as leukodystrophy. Abnormal brain development and leukodystrophy likely underlie the neurological abnormalities that occur in D-bifunctional protein deficiency. HSD17B4 ...
    https://medlineplus.gov/.../d-bifunctional-protein-deficiency - Genetics
  5. HSD17B4 gene 
    ... in the brain and spinal cord; loss of white matter is described as leukodystrophy. Abnormal brain development and leukodystrophy likely underlie the neurological abnormalities that occur in D-bifunctional protein deficiency. More ...
    https://medlineplus.gov/genetics/gene/hsd17b4 - Genetics
  6. Peroxisomal acyl-CoA oxidase deficiency 
    ... of myelin-containing tissue (white matter) in the brain and spinal cord; loss of white matter is described as leukodystrophy. Leukodystrophy is likely involved in the development of the neurological abnormalities that occur in peroxisomal acyl-CoA oxidase deficiency. ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics
  7. ACOX1 gene 
    ... of myelin-containing tissue (white matter) in the brain and spinal cord; loss of white matter is described as leukodystrophy. Leukodystrophy is likely involved in the development of the neurological abnormalities that occur in peroxisomal acyl-CoA oxidase deficiency. ...
    https://medlineplus.gov/genetics/gene/acox1 - Genetics
  8. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... parts of the body. Some affected individuals have abnormalities of brain structures, such as the tissue that connects the left and right halves of the brain (the corpus callosum), a tissue called white matter, the fluid-filled cavities (ventricles) near the center ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  9. Desmosterolosis 
    ... to a few words or phrases. Common brain abnormalities in desmosterolosis include malformation of the tissue that connects the left and right halves of the brain (the corpus callosum) and loss of white matter, which consists of nerve fibers covered by a ...
    https://medlineplus.gov/genetics/condition/desmosterolosis - Genetics
  10. Cranial Ultrasound Video (Radiological Society of North America) (American College of Radiology)  
    ... IVH). assess whether there is damage to the white matter brain tissue surrounding the edges of the ventricles, a condition known as periventricular leukomalacia (PVL). evaluate for congenital abnormalities. locate the site of an infection or tumor. ...
    https://www.radiologyinfo.org/en/info/ultrasound-cranial - Videos
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