Recensioni verificate Soddisfatta del servizio.
Personale disponibile e gentile. Lo consiglio a tutti ...
Cliente Sorgente Genetica
logomysorgente

02  4948  5291

  • Cos'è AURORA

    Aurora è il test di screening prenatale di ultima generazione 
    sicuro, affidabile,
    veloce e precoce

  • Sicuro

    Grazie a un semplice prelievo di sangue materno
    eviti il rischio di aborto di tecniche invasive come amniocentesi o villocentesi

  • Affidabile

    Oltre il 99,9% di affidabilità nel rilevare
    la trisomia 21, responsabile
    della Sindrome di Down

  • Precoce e veloce

    icona svegliaIndividuare precocemente la presenza di anomalie cromosomiche è fondamentale:
    puoi effettuare Aurora dalla 10ª settimana

    icona documentoIl test è veloce: risultati in 7-10 giorni lavorativi con la percentuale di test da ripetere più bassa del mercato: 0,1%

  • La serenità della mamma
    in 3 semplici passi

    icotelefona

    Prenota il test

    icoesami

    Fai un prelievo di sangue

    icoginecologo

    Leggi i risultati

  • Test diagnosi prenatale non invasivo
  • 151126 banner Aurora mobile 01
  • 151126 banner Aurora mobile 02
  • 151126 banner Aurora mobile 03
  • slide mobile03
cover cartoon
cover venturetti

Ultime notizie dal mondo della genetica


Progression of Huntington's disease slowed

Professor Sarah Tabrizi of the University of London announced the first positive results in the fight against Huntington's disease. Phase 1 of trials for a new drug was successful. Treatment has slowed the progression of the genetic disease, offering for the first time a concrete hope. In fact, current treatments only allow the symptoms to be mitigated, but they do not affect the disease itself.

The drug is composed of a strip of synthetic DNA, adaptable also to other neurodegenerative diseases. The approach could therefore offer hope also against Alzheimer's and Parkinson's. For the time being, however, the results only concern Huntington's disease.

Huntington's disease is caused by an inherited genetic variation. The defective gene gives instructions to produce a toxic protein, copied from messenger molecules and spread in the brain. The drug is called Ionis-HTTRx and intercepts the molecules, destroying them before the protein spreads. The administration involves an injection directly into the fluid surrounding the spinal cord. In this way the drug reaches the brain and does not disperse.

Phase 1 of the trial involved 46 women and men in the early stages of the disease. The doctors injected four doses of the drug half a month away from each other. With each injection, they increased the dosage. The other half received a placebo. Subjects who received the drug showed a decrease in protein levels.
Although the results are positive and bode well, a broader study will be needed to confirm them.

Source: theguardian.com

Link social

Link social