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Cáncer hereditario
Customer area
  • Products and Services
    • Prenatal stage
      • Non-Invasive Prenatal Test
      • Prenatal diagnosis
      • Prenatal diagnosis of a rare disease
    • Pediatric stage
      • Neuropaediatric disorders
      • Genetic syndromes
      • Diagnosis of rare diseases
    • Adult stage
      • Diagnosis of rare diseases
      • Reproductive screening
      • Cancer
    • IMEXOME
    • Kits for analysis
  • Hospitals and Specialists
    • Kits for analysis
    • Techniques available
  • Patients and Families
    • Genetic guide
    • Non-Invasive Prenatal Test
  • R&D
    • Partner profile
    • R&D projects
  • About us
    • About us
    • Team
    • Excellent quality
HomeProducts and ServicesPrenatal stage

Prenatal stage

The prenatal stage covers the period from fertilisation to birth.

Pregnancy is a stage of life filled with expectations and great hopes for the future, although doubts and uncertainties, which may become critical, can also arise.

Congenital defects are one of the leading causes of morbidity/mortality in modern developed societies such as ours. In addition, delayed motherhood increases the risk of some common congenital diseases such as Down’s syndrome.

Congenital defect prevention programmes play a key role in improving the health status of the population (WHO).

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Products:

Prenatal Test

Non-Invasive

Prenatal

of a rare disease

CGX

Arrays

What is a congenital defect?

Congenital defects are abnormalities in morphological, structural, functional or molecular development that are present at birth, whether hereditary or not. Such abnormalities may appear after birth.

 

Non-Invasive Prenatal Test

In contrast to techniques such as amniocentesis or chorionic villus sampling, a non-invasive prenatal genetic study uses a blood sample to analyse foetal DNA…

Prenatal diagnosis

Rare diseases have a low incidence in the population of less than 1 in every 200 inhabitants…

Prenatal diagnosis of a rare disease

Whenever a rare disease is diagnosed in a family, it is essential to try to identify the genetic cause of that disease…

Techniques available

IMEGEN use the most accurate and up-to-date genetic analysis techniques. The optimal diagnostic efficacy is obtained by selecting the most appropriate technique for each clinical case.

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    Instituto de Medicina Genómica, S.L.

    Founded in 2009 by a team of scientists with more than 20 years’ business experience, it has since grown to become the leader in the genetics and genomics sector.

    Meet Imegen

    • Products and Services
      • Prenatal stage
        • Non-Invasive Prenatal Test
        • Prenatal diagnosis
        • Prenatal diagnosis of a rare disease
      • Pediatric stage
        • Neuropaediatric disorders
        • Genetic syndromes
        • Diagnosis of rare diseases
      • Adult stage
        • Diagnosis of rare diseases
        • Reproductive screening
        • Cancer
      • IMEXOME
      • Kits for analysis
    • Hospitals and Specialists
      • Kits for analysis
      • Techniques available
    • Patients and Families
      • Genetic guide
      • Non-Invasive Prenatal Test
    • R&D
      • Partner profile
      • R&D projects
    • About us
      • About us
      • Team
      • Excellent quality

    Contact

    c/ Agustín Escardino 9, Parc Científic de la Universitat de València - 46980 Paterna

    info@imegen.es
    Tel: +34 963 212 340

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