Phenotype #0000024906

Individual ID	00028666
Associated disease	PVNH1
Phenotype details	periventricular heterotopia, type 1/frontometaphyseal dysplasia; delayed closure anterior fontanel, craniofacial anomalies, marked genua valga necessitating surgical corrections; 5y-MRI cranial bilateral PVNHs; no seizures, normal motor/mental development; 8y-radiological FMD
Diagnosis/Initial	-
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Yu Sun
Database submission license	No license selected
Created by	Yu Sun
Date created	2009-08-12 12:45:12 +02:00 (CEST)
Date last edited	N/A

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