Lynch Syndrome & Colorectal Cancer : Learn more
All patients with colorectal (CRC) [DG27] and endometrial cancer [DG42] should now receive genetic testing according to NICE guidelines.
Come and learn how you can achieve that for your patients.
All patients with colorectal (CRC) [DG27] and endometrial cancer [DG42] should now receive genetic testing according to NICE guidelines.
Come and learn how you can achieve that for your patients.
All patients with colorectal (CRC) [DG27] and endometrial cancer [DG42] should now receive genetic testing according to NICE guidelines.
Come and learn how you can achieve that for your patients.
If you have questions about how to order Whole Genome Sequencing for your patients with suspected rare diseases, then drop into our online sessions and get the answers. The South East Genomics team will be available to answer all your questions on July 7th from 11 – 11:45am. Do you need support to navigate your …
All your questions about ordering Whole Genome Sequencing for rare diseases answered Read More »
All patients with colorectal (CRC) [DG27] and endometrial cancer [DG42] should now receive genetic testing according to NICE guidelines.
Come and learn how you can achieve that for your patients
Synnovis Genomics Laboratory (Guy’s Hospital) Service Update Dear Service User, On 15th August 2022 we wrote to you to explain that some of our generic service email inboxes were unavailable following the Guys and St Thomas’ Hospitals wide IT outage; we provided a list of alternative email addresses to be used to contact the laboratory. …
Synnovis Genomics Laboratory (Guy’s Hospital) Service Update Read More »
Session Fifth: Spinal Muscular Atrophy Spinal muscular atrophy (SMA) is a genetic condition affecting the central nervous system, peripheral nervous system, and voluntary muscle movement (skeletal muscle). During this session we will hear from professionals in the field on SMA management, genetic testing, and treatments available as well as hearing from a patient advocate. Agenda: …
Lunch and Learn: Think Patient Care, Think Genomics Read More »
Lynch syndrome (LS) is an inherited condition caused by pathogenic variants in DNA genes which result in an increased risk of colorectal, endometrial, and other cancers. LS affects approximately 1 in 300-1 in 400 people, with 200,000-300,000 people likely to have this condition in the UK. It is estimated that only 5% of people with …
Lynch syndrome (LS) is an inherited condition caused by pathogenic variants in DNA genes which result in an increased risk of colorectal, endometrial, and other cancers. LS affects approximately 1 in 300-1 in 400 people, with 200,000-300,000 people likely to have this condition in the UK. It is estimated that only 5% of people with …
Whole Genome Sequencing Drop In Session: Tuesday 11th October, 14:30-15:30 Are you a clinician looking to find out more about Whole Genome Sequencing (WGS)? Then this drop-in session is for you! During the session you will find out more information on this new testing, how it can be used for your patients and have the …