BIOCHEMICAL TESTS AND EXPANDED METABOLIC SCREENING

Biochemical tests and expanded metabolic screening

  1. Acylcarnitine quantitative profile in plasma
  2. Amino acids analysis in plasma
  3. Rhizomelic condrodistrofia punctata
  4. Ankylosing Spondylitis (inmunologic flow cytometry) (HLA-B27)
  5. Fabry disease: Alpha- Galactosidase A enzyme activity
  6. Fabry disease: Globotriaosylceramide, Gb3
  7. Cystic fibrosis (100 mutations panel)
  8. Sperm DNA fragmentation
  9. MPS, screen- Electrphoresis & quantitation  in urine
  10. MPS, quantitative in urine
  11. Lysosomal storage disease: panel enzyme activity (13 enzymes)
  12. Preeclampsia test (sFlt-1, PIGF, Indice)
  13. Newborn screening panel (50 diseases)
  14. Newborn screening panel more screening for lysosomal storage disorders  (LSD)
  15. Newborn screening panel more screening for sevre combined imnmunodeficiency  (SCID)
  16. Others

Sample requirements for biochemical testing

  1. The requirements vary depending on the test samples. Please call customer service (00507) 7742871 to request such samples and requirements depending on the examination required.
  2. Sample shipping address: Attention: Oriana Batista, M.Sc., Dr.rer.nat.
    Centro Gendiagnostik
    Avenida Central, Contiguo al Cuartel de Bomberos
    David, Provincia de Chiriquí
    Panamá
  3. For questions, please contact Client Services at (00507) 7742871.

Request form for biochemical testing

Send the requisition form together with the sample and copy of payment verification. Fill the requisition form completely.Descargar formulario para solicitar pruebas bioquímicas.

La mutación G202A, en hijo hemicigoto (arriba) y madre heterocigota (abajo). Esta mutación acompañada de la mutación A376G ó T968C definen la variante africana negativa.

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Arriba se muestra el resultado de un niño hemicigoto para la variante africana negativa, caracterizada por las mutaciones A376G y G202A, y abajo de una niña heterocigota para la variante Mediterránea, definida por la mutación C563T.

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The G202A mutation, in the hemizygous son (above) and heterozygous mother (below). This
mutation accompanied with the A376G mutation or T968C define the african negative variant.

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Above the result of a hemizygous child with the african negative variant , characterized by
mutations A376G and G202A , and below a heterozygous girl with the mediterranean variant, defined by the C563T mutation

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