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This fund is designed for donors who wish to contribute but are unable to select a specific campaign. It operates through monthly subscription donations via card, PayPal, or one-time contributions via IBAN. The fund supports the medical treatment of children under 18 years of age who are battling cancer or require a kidney, liver, or heart transplant.
This fund is designed for donors who wish to contribute but are unable to select a specific campaign. It operates through monthly subscription donations via card, PayPal, or one-time contributions via IBAN. The fund supports the medical treatment of children under 18 years of age who are battling cancer or require a kidney, liver, or heart transplant.
За изследвания в Турция. След консултация с лекарския отдел предавам плана на лечение.На пациента е поставена предварителна диагноза CMT, но генетичните изследвания все още не са завършени. Като за начало е необходимо да се направи соло пълно геномно секвениране (WGS).
Цената на изследването е 3500 евро.CMT е генетично хетерогенно заболяване и до момента са идентифицирани множество подтипове, свързани с различни гени. Поради тази причина, за да се потвърди диагнозата и да се изготви подходящ план за лечение и проследяване, е необходимо да се извърши соло пълно геномно секвениране.
WGS анализира цялата геномна последователност само от пробата на пациента с цел откриване на потенциално патогенни варианти. Чрез този метод могат да бъдат идентифицирани генетични мутации, които не са били открити при предишни изследвания.CMT е генетично хетерогенно заболяване и до момента са идентифицирани множество подтипове, свързани с различни гени. Поради тази причина, за да се потвърди диагнозата и да се изготви подходящ план за лечение и проследяване, е необходимо да се извърши соло пълно геномно секвениране.
WGS анализира цялата геномна последователност само от пробата на пациента с цел откриване на потенциално патогенни варианти. Чрез този метод могат да бъдат идентифицирани генетични мутации, които не са били открити при предишни изследвания.For research in Turkey. After consultation with the medical department, I am handing over the treatment plan.The patient has been given a preliminary diagnosis of CMT, but genetic testing has not yet been completed. To begin with, a solo whole genome sequencing (WGS) needs to be performed. The cost of the study is 3500 euros.CMT is a genetically heterogeneous disease and so far multiple subtypes associated with different genes have been identified. For this reason, in order to confirm the diagnosis and to design an appropriate treatment and follow-up plan, solo whole genome sequencing is necessary. WGS analyses the whole genome sequence from the patient sample alone in order to detect potentially pathogenic variants. Genetic mutations that have not been detected in previous studies can be identified using this method.CMT is a genetically heterogeneous disease and multiple subtypes associated with different genes have been identified to date. For this reason, in order to confirm the diagnosis and to design an appropriate treatment and follow-up plan, solo whole genome sequencing is necessary. WGS analyses the whole genome sequence from the patient sample alone in order to detect potentially pathogenic variants. Genetic mutations that have not been detected in previous studies can be identified using this method.
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PavelAndreev.ORG is an international platform for organizing fundraising campaigns managed by the Pavel Andreev Foundation. Headquarters: Bulgaria, Varna, 113 General Kolev Blvd., Nikulitsel Building, company No. 206678629. All donations made through the platform are collected and administered in Bulgaria by the Foundation team. The campaigns are also managed by the central team in Bulgaria. At the moment, the organization is not registered as a local entity in other countries.
Дари живот на Дария
Give life to Daria
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