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Results 1 - 10 of 26 for Macrogyria
  1. Isolated lissencephaly sequence (ILS) is a condition that affects brain development before birth. Normally, the cells that make up the exterior of the brain (cerebral ...
  2. Lissencephaly with cerebellar hypoplasia (LCH) affects brain development, resulting in the brain having a smooth appearance (lissencephaly) instead of its normal folds ...
  3. X-linked lissencephaly with abnormal genitalia (XLAG) is a condition that affects the development of the brain and genitalia. It occurs most often in males. ...
  4. ... by a pattern of abnormal brain development called lissencephaly. Normally, the surface of the brain (cerebral cortex) has folds and grooves. Lissencephaly causes the surface of the brain to be ...
  5. ... PAFAH1B1 gene have been found to cause isolated lissencephaly sequence (ILS), a condition characterized by abnormal brain ... results in the brain having a smooth surface (lissencephaly) instead of its normal folds and grooves. Individuals ...
  6. ... DCX gene have been found to cause isolated lissencephaly sequence (ILS). This condition is characterized by abnormal ... results in the brain having a smooth surface (lissencephaly) instead of its normal folds and grooves. Individuals ...
  7. ... condition typically have a brain abnormality called cobblestone lissencephaly, in which the surface of the brain lacks ... that this problem with neuronal migration causes cobblestone lissencephaly in children with Walker-Warburg syndrome. Less is ...
  8. Birth Disorders of the Brain and Spinal Cord From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Brain Diseases/Specifics ... Brain Diseases ... Neural Tube Defects/Specifics ... Neural Tube Defects ... Hydrocephalus/Specifics ... Hydrocephalus ... Brain Malformations/Specifics
  9. The ADGRG1 gene, formerly known as GPR56, provides instructions for making a protein that is critical for normal brain development. Before birth, the ADGRG1 ...
  10. ... does not have the normal folds and grooves (lissencephaly). The signs and symptoms of Miller-Dieker syndrome ... region. The loss of the PAFAH1B1 gene causes lissencephaly. Lissencephaly is associated with severe intellectual disabilities, developmental ...
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