eXTReMe Scraping API| URL: | https://genlab.gr  (UTC) |
| Request ID: | 2026-04-12-02-44-02-XmGQT0h4shYJd47Amxw3 |
| Scraper Location: | EU |
| Scrape Status: | Success View Full API JSON |
 |
|
|
| Title: Genesis Genoma Lab - Ιατρικό Εργαστήριο - Χαλάνδρι |
| Description: Εξασφαλίζουμε άμεση και αξιόπιστη διάγνωση. Στόχος μας είναι η όσο το δυνατόν ευρύτερη κάλυψη των αναγκών του γενετικού ελέγχου, καθώς και η παροχή υπηρεσιών κλινικής γενετικής και γενετικής συμβουλευτικής. |
| Top 25 Nouns: genesis genoma genlab course covid19 exome sarscov2 sequencing cnvs copy corona coronavirus2 disease internet number prenatal respiratory site syndrome variants virus |
| Category | Domain | Compliancy Score Higher is better |
Tracking Cookies Before / Accept / Necessary Consent |
Tracking Pixels Before / Accept / Necessary Consent |
Cookie Banner | |
|---|---|---|---|---|---|---|
| Healthcare |  |
genlab.gr |
8919 | 0 / - / - | 4 / - / - | Not Found |
| Domain | Compliancy Score Before / Accept / Necessary Consent |
|---|
|
Healthcare |
8919 |
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| Cookie Banner Necessary Only Button Found | No |
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| GCM V2 Advanced Mode Found | No |
| GCM V2 Misconfiguration Found | Yes |
| Bing Ads UET Consent Mode Found | No |
Before / Accept / Necessary Consent | |
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Before / Accept / Necessary Consent | |
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| Top 25 Nouns: genesis genoma genlab course covid19 exome sarscov2 sequencing cnvs copy corona coronavirus2 disease internet number prenatal respiratory site syndrome variants virus | |
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| google_ | -48 |
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Before Consent:
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After Accept All Consent:
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"innerText" : "Στα γενετικά νοσήματα περιλαμβάνονται όλες οι διαταραχές που οφείλονται σε ανωμαλίες του γονιδιώματος (μεταλλάξεις, χρωμοσωμικές ανωμαλίες, ελλείμματα/διπλασιασμοί χρωμοσωμικών περιοχών). Ορισμένα γενετικά νοσήματα κληρονομούνται από τους γονείς, ενώ άλλα οφείλονται σε νέες μεταλλάξεις. Τα γενετικά νοσήματα διακρίνονται σε μονογονιδιακά (π.χ. μεσογειακή αναιμία, κυστική ίνωση), πολυπαραγοντικά (π.χ. καρδιοπάθειες, καρκίνος, νόσος Alzheimer), μιτοχονδριακά (π.χ. Σύνδρομο Kearns – Sayre, σύνδρομο MELAS) και σε χρωμοσωμικές ανωμαλίες (π.χ. σύνδρομα Down, Turner, Klinefelter)."
},
{
"innerText" : "Η νόσος COVID-19 (Corona Virus Disease – 19), που προκαλείται από τον νέο κορωνοϊό SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus-2), ξεκίνησε τον Δεκέμβριο του 2019 στην περιοχή Γιουχάν της Κίνας και έκτοτε έχει διασπαρεί σχεδόν σε όλο τον κόσμο."
},
{
"innerText" : "Αποτελεί ένα νέο στέλεχος κορωνοϊού που δεν είχε προηγουμένως ανιχνευθεί στον άνθρωπο."
},
{
"innerText" : "Για το Μοριακό έλεγχο του Covid-19:"
},
{
"innerText" : "Το εργαστήριο διαθέτει σύγχρονο εξοπλισμό, όπως αυτόματους αναλυτές, συστήματα μοριακής και κυτταρογενετικής ανάλυσης, αλληλούχησης νέας γενιάς (NGS), προεμφυτευτικoύ γενετικού ελέγχου (PGS) και μοριακού καρυοτύπου."
},
{
"innerText" : "Η κυστική ίνωση είναι το δεύτερο συχνότερο κληρονομικό νόσημα στην Ελλάδα με συχνότητα φορέων 4-5%. Ο έλεγχος συστήνεται σε όλα τα ζευγάρια πριν ή κατά τη διάρκεια των πρώτων εβδομάδων της κύησης με ανάλυση ολόκληρου του υπεύθυνου γονιδίου."
},
{
"innerText" : "Το Prenatal SAFE Karyo είναι το επόμενο επίπεδο στο μη επεμβατικό προγεννητικό έλεγχο και προσφέρει τη δυνατότητα ανάλυσης όλων των χρωμοσωμάτων του εμβρύου με μια απλή αιμοληψία."
},
{
"innerText" : "Ο προγεννητικός χρωμοσωμικός έλεγχος με μοριακό καρυότυπο είναι μια νέα μέθοδος της μοριακής κυτταρογενετικής που έχει στόχο να μειώσει τα ποσοστά γεννήσεων παιδιών με σοβαρά γενετικά νοσήματα. Ανιχνεύει αριθμητικές χρωμοσωμικές ανωμαλίες (τρισωμίες, μονοσωμίες) καθώς και μικρού μεγέθους αλλαγές αριθμού αντιγράφων (Copy Number Variants, CNVs), οι οποίες δεν μπορούν να ανιχνευθούν με τις συμβατικές κυτταρογενετικές τεχνικές και συνδέονται, μεταξύ άλλων, με την εμφάνιση συγγενών ανωμαλιών, νοητικής υστέρησης και αυτισμού."
},
{
"innerText" : "Το Whole exome sequencing είναι μία μοριακή τεχνική τελευταίας αιχμής που επιτρέπει την αλληλούχιση της κωδικοποιούσας περιοχής όλων των γονιδίων του γονιδιώματος. Συνιστάται συνήθως σε ασθενείς που παρουσιάζουν πολύπλοκο φαινότυπο, γεγονός που καθιστά δύσκολη τη στόχευση συγκεκριμένων γονιδίων. Μπορεί να πραγματοποιηθεί είτε έλεγχος του πάσχοντα, είτε ταυτόχρονος έλεγχος του πάσχοντα και των γονέων του."
},
{
"innerText" : "Το εργαστήριο Genesis Genoma Lab στελεχώνεται από Γενετιστές και Βιολόγους με ολοκληρωμένη κλινική και εργαστηριακή εμπειρία στη διάγνωση και αντιμετώπιση των γενετικών νοσημάτων."
},
{
"innerText" : "Το εργαστήριο Genesis Genoma συμμετέχει ως βασικός συντελεστής στην πραγματοποίηση του μικτού εξ αποστάσεως επιμορφωτικού προγράμματος «Ιατρική Γενετική» που προσφέρεται για πρώτη φορά στην Ελλάδα και υλοποιείται από το Κέντρο Δια Βίου Μάθησης του Πανεπιστημίου Ιωαννίνων, με επιστημονικό υπεύθυνο τον Καθηγητή της Ιατρικής Σχολής του Πανεπιστημίου Ιωαννίνων, Ιωάννη Γεωργίου."
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{
"innerText" : "Το βασικό σκέλος της επιμόρφωσης (διάρκειας 32 εβδομάδων) πραγματοποιείται εξ αποστάσεως, σε ειδικά διαμορφωμένη πλατφόρμα ηλεκτρονικής μάθησης, ενώ η εργαστηριακή πρακτική άσκηση λαμβάνει χώρα στις υψηλής ποιότητας εγκαταστάσεις του εργαστηρίου μας."
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{
"innerText" : "Εκεί δίνεται η μοναδική δυνατότητα στους εκπαιδευόμενους να αποκτήσουν πρακτική εμπειρία στο αντικείμενο της Γενετικής Ιατρικής…"
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{
"innerText" : "Δευτέρα με Παρασκευή, από τις 08:30 έως τις 15:30."
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"innerText" : "Όχι, για την πραγματοποίηση γενετικών αναλύσεων δεν απαιτείται προηγούμενη νηστεία και δεν επηρεάζονται από την ώρα της ημέρας που θα γίνει η αιμοληψία."
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"innerText" : "Το εργαστήριο παραλαμβάνει δείγματα Δευτέρα με Παρασκευή, από τις 08:30 έως τις 16:00 και μέχρι τις 20:00 μετά από συνεννόηση."
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"innerText" : "Όχι, πρέπει να συνεννοηθείτε με το γυναικολόγο σας για τη λήψη του δείγματος. Το δείγμα μπορείτε να το φέρετε στο εργαστήριο ή να το παραλάβουμε εμείς από το λήπτη ιατρό."
},
{
"innerText" : "Όχι. Ο Καθηγητής Ιατρικής Γενετικής Ε. Καναβάκης και η Καθηγήτρια Γενετικής Α. Μαύρου είναι διαθέσιμοι για Γενετική Συμβουλευτική πριν και μετά τη διεξαγωγή γενετικών αναλύσεων στο κέντρο μας χωρίς επιπλέον κόστος."
},
{
"innerText" : "Το εργαστήριο Genesis Genoma Lab στελεχώνεται από Γενετιστές και Βιολόγους με ολοκληρωμένη κλινική και εργαστηριακή εμπειρία στη διάγνωση και αντιμετώπιση των γενετικών νοσημάτων."
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