Phenotype #0000059458

Individual ID	00079747
Associated disease	-
Phenotype details	severe pre- and postnatal growth failure, sensorineural deafness, mental retardation; insulin-like growth factor I deficiency; mild myopia; behavioral difficulties, hyperactivity, short attention span; no skeletal abnormalities; micrognathia, bilateral ptosis,; low hearline, bilateral clinodactyly, single palmar crease,
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Hermine van Duyvenvoorde
Database submission license
Created by	Hermine van Duyvenvoorde
Date created	2008-09-19 15:45:50 +02:00 (CEST)
Date last edited	2009-08-07 16:09:22 +02:00 (CEST)

Global Variome shared LOVD