Phenotype #0000220840

Individual ID 00285820
Associated disease -
Phenotype details severe motor dysphasia, difficulties in chewing and swallowing, continuous drooling, accompanied by hemiparesis, microcephaly and progressive kyphoscoliosis, severe expressive speech dyspraxia, poor communication skills, could write simple words and could communicate
Diagnosis/Initial -
Inheritance -
Diagnosis/Definite -
Age/Examination 00y08m (8 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Laurent Villard
Database submission license No license selected
Created by Laurent Villard
Date created 2020-02-12 11:27:36 +01:00 (CET)
Date last edited 2020-02-29 10:18:01 +01:00 (CET)

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