Phenotype #0000323889

Individual ID 00433368
Associated disease microcephaly
Diagnosis/Initial primary microcephaly
Diagnosis/Definite -
Phenotype details primary microcephaly; birth OFC (SD-2), weigth median, length (SD1); OFC (SD-3), weigth (SD+1.5), length (SD3); g4y-eneralized, absences, treatment VPA; moderate intellectual disability; MRI simplified pattern; birth OFC (SD-2), weigth median, length (SD1); OFC (SD-3), weigth (SD+1.5), length (SD3); g4y-eneralized, absences, treatment VPA; moderate intellectual disability; MRI simplified pattern
Inheritance Familial, autosomal recessive
Age/Examination 5y6
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 2023-03-06 14:23:39 +01:00 (CET)
Date last edited N/A

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