Phenotype #0000117392

Individual ID 00144655
Associated disease MRMV1
Phenotype details Parry-Romberg syndrome. Could suppress the CMM partially so that she was able to write bimanually with a computer keyboard. There were no CMM of her feet.
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
MotorSkills -
Severity_score Woods & Teuber 2
Protein -
Brain/Imaging MRI
Owner name Tatjana Bierhals
Database submission license No license selected
Created by Tatjana Bierhals
Date created 2017-12-19 10:22:42 +01:00 (CET)
Date last edited 2020-01-10 12:28:57 +01:00 (CET)

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