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SMN Muscular Atrophy is an inherited disease caused by mutations in the SMN1 (Survival of Motor Neuron) gene.
It is the most common genetic cause of childhood mortality and occurs when the child has inherited mutated genes (SMN1) from both parents.
The disease causes gradual degeneration of the lower motor neurons of the spinal cord and is appeared in the child with ever-increasing muscle weakness and muscle atrophy.
Genetic testing is recommended as a part of the woman's preventive prenatal check-up.
The results determine the need or not for:
INFORMATION FOR LABORATORY CHECK
A simple blood test is required for laboratory testing.
No preparation or diet is required. Blood sampling can be done at any time of the day.
Blood sampling can be done at any time of the day (laboratory hours 7.30 a.m. – 7.30 p.m.).
EXPECTED TIME FOR THE RESULTS
Results are given within 12 working days.
According to our latest update to EOPYY, it is NOT prescribed
The cost of the laboratory test is 140 euros.
Information selected - indicative with sources: Interpretation of Diagnostic Tests - J.Wallach and https://labtestsonline.org
The choice and explanation of the use of the analysis is the exclusive responsibility of your doctor
Edited by : Ioannis Grattisia Head of Laboratory / MSc Clinical Biochemistry - Molecular Biology
2022 - 2023
Diagnostic: Director Biochemist I. Gratsia - Biopathologist I. Katsavochristos / M. Kolokouri - Radiologist S. Alagiannis
Doctors: General Practitioner X. Chrysanthaki - Endocrinologist E. Typhoxylou – Cardiologist A. Castanas - Neurologist C. Karagiorgis - Urologist K. Psyllias - Pulmonologist Zafiria Barbaressou
Liability & Responsibility Ethics in Biomedical Science - Personalised Medical Practice with Courtesy and Empathy
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