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Experimental model and subject details Patients Patients were aged between 3 and 16 years old with the exception of P6 being 36 years old and were included based on molecular diagnosis of biallelic loss of function mutations in SAMHD1 , RNASEH2B or ADAR1 genes for AGS or dominant-negative mutation in COPA gene for patients with COPA disease

A prospective study in 100 patients

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With GBS, the patient should be closely monitored with these tests and checks: Neurological checks Oxygenation monitoring Pulmonary function evaluation Vital sign checks Make sure to order frequent neurological and vital sign checks for your patients with GBS, as well as frequent evaluation of respiratory effort