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Macrogyria
- 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 ...
- Lissencephaly with cerebellar hypoplasia (LCH) affects brain development, resulting in the brain having a smooth appearance (lissencephaly) instead of its normal folds ...
- 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. ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- Birth Disorders of the Brain and Spinal Cord (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
- The ADGRG1 gene, formerly known as GPR56, provides instructions for making a protein that is critical for normal brain development. Before birth, the ADGRG1 ...
- ... 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 ...