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 Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons 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)

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