Phenotype #0000331344

Individual ID 00441961
Associated disease MLC
Phenotype details macrocephaly; mildly delayed early motor development; 26m-walk; delayed language development; 3y-detoriation; seizures,; cognitive; decline; still ambulant; 3y-seizures; OFC >98perc.; dysarthria; no dysphagia; no spasticity arms; cerebellar ataxia arms; spasticity legs; cerebellar ataxia legs
Diagnosis/Initial classical megalencephalic leukoencephalopathy with subcortical cysts
Inheritance Familial, autosomal recessive
Diagnosis/Definite MLC2A
Age/Examination 6y (6 years)
Age/Diagnosis -
Age/Onset <1y
Phenotype/Onset -
Protein -
Owner name Rogier Min
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-10-31 16:41:00 +01:00 (CET)
Date last edited N/A

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