THE INTERNATIONAL SOCIETY FOR GASTROINTESTINAL HEREDITARY TUMOURS
InSiGHT
improve knowledge in the means of prevention, treatment and early detection of gastrointestinal hereditary tumour syndromes (GHTS) and any condition resulting in GHTS and relief of sickness of those suffering from GHTS and their familes; and the advancement of education of the public in GHTS to include the education of physicians and others in the molecular genetics and clinical management of GHTS
1139700
IČO
2011
Založeno
NW10 7NS
Adresa
insight-group.org
Web
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Více Nemoci specifických orgánů
Poslední komentáře
So inspiring to see organizations like InSiGHT working tirelessly to improve the lives of families affected by gastrointestinal hereditary tumours! Let's raise awareness together! 💚 #GeneticHealth #InSiGHTdetail |
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Excited for the upcoming biennial meeting in Singapore! Looking forward to collaborating with fellow professionals to advance our understanding of GHTS. Together, we can make a difference! 🌍❤️ #HealthcareInnovation #InSiGHT2026detail |
Poslední diskuze
1. What innovative strategies can NGOs employ to raise awareness about hereditary gastrointestinal tumours among the general public and healthcare professionals?Odpovědí: 3, Naposledy před 1 den detail |
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2. How can collaboration between genetic researchers and clinicians improve the outcomes for patients with hereditary gastrointestinal tumours?Odpovědí: 3, Naposledy před 1 den detail |
V okolí
4.5
Reviews
NW10 7NS
Místo
O společnosti
- G40, T20, H21 -
The International Society for Gastrointestinal Hereditary Tumours InSiGHT is a multidisciplinary scientific organisation whose mission is to improve the care of patients and families worldwide with any hereditary condition resulting in gastrointestinal tumours. Syndromes Most hereditary gastrointestinal tumours occur as part of a distinct inherited syndrome. Each of these is due to alteration in a specific gene or one of a group of genes and has a characteristic set of clinical features. Variants A key part of our work is understanding the relationship between genetic alterations genotype and disease phenotype.
Nemoci specifických orgánů Soukromé nadace poskytující granty
23 Vacancy
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