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Spinal Muscular Atrophy SMN

SMN Muscular Atrophy is an inherited disease caused by mutations in the SMN1 (Survival of Motor Neuron) gene.

Spinal Muscular Atrophy SMN Prenatal molecular testing in Spinal Muscular Atrophy- SMN gene Price 140 euros | Check Up Medicus

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:

  1. complementary testing of the partner in the SMN1 gene
  2. testing of the fetus in case the spouse has an SMN1 mutation



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.).


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

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

Biopathology Diagnostic Laboratory | Microbiological | Molecular | DNA | Ultrasonic | EOPYY – Clinic

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