Phenotype #0000059473

Individual ID 00079762
Associated disease -
Phenotype details insulin-like growth factor I deficiency; neurology normal; Bilateral hearing loss, hyperlaxity of joints; Dimples in lumbar region; Triangular face, low placed posterior rotated ears, medial flaring eyebrows; Hypertelorsim, bilateral clinodactyly; delayed dentition and hypocanthal folds
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Patricia Willemse
Database submission license No license selected
Created by Patricia Willemse
Date created 2009-06-19 12:21:41 +02:00 (CEST)
Date last edited 2009-07-17 17:07:09 +02:00 (CEST)

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