Microspherophakia / Megalocornea / primary congenital Glaucoma / Weill-Marchesani syndrome 3 recessive type

Genetic test Export to PDF
Full name:
Microspherophakia / Megalocornea / primary congenital Glaucoma / Weill-Marchesani syndrome 3 recessive type
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Method technique:
Laboratory:
RIZIV code:
Turnaround time (maximum):
8 weeks
Document(s):
Created:
31 Jul 2019 - 11:23
Changed:
20 May 2022 - 09:56