Periventricular Heterotopia
What's New
Last Posted: Mar 10, 2023
- Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders.
González-Morón Dolores, et al. PloS one 2017 0 (9) e0185103 - Epilepsy phenotypes associated with MAP1B-related brain malformations.
Arya Ravindra, et al. Epileptic disorders : international epilepsy journal with videotape 2021 0 (2) 392-396 - Periventricular heterotopia
From NCATS Genetic and Rare Diseases Information Center - X-linked periventricular heterotopia
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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