Phenotype #0000283615

Individual ID 00390077
Associated disease MRMV
Phenotype details hypoplastic corpus callosum, asymmetric ventriculomegaly, dysgyria and polymicrogyria, dysmorphic basal ganglia, hypoplastic disorganized vermis, hypoplastic asymmetric brain stem; no developmental delay; regular school; OFC -2 SD; no epilepsy; mild terminal kinetic tremor bilaterally; no dystonia
Diagnosis/Initial congenital mirror movement
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 10y (10 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-11-09 17:45:02 +01:00 (CET)
Date last edited N/A

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