Istanbul Faculty of Medicine Rare Diseases Research Laboratory opened
ISTANBUL (UAV) – Istanbul medical School Rare Diseases Research Laboratory opened
prof. Dr. Gülden Gökçay: “In rare environments, 80 of them are children of children”
ISTANBUL – 300 million in the world, TurkeyOn the other hand, about 5 million people in Turkey are housed within the Istanbul Faculty of Medicine. Istanbul University at the opening Child Health Head of Rare Diseases Department of the Institute, Prof. Dr. 3.5 million of them are children. In rare environments, 80 of them are children,” he said.
7 thousand rare measurement examinations related to 300 million people in the world and 5 million people in Turkey are located in the education faculty of the ‘Napa Diseases Research’ at the Istanbul University-Istanbul University Faculty of Medicine. The ceremony was attended by Zanzibar Deputy Wanu Hafidh Ameir, daughter of Tanzanian President Samia Suluhu Hassan, donors of the laboratory Mukaddes and Ziya Karahan couple, Dean of Istanbul Medical Faculty Prof. Dr. Tufan Tükek, Istanbul Chief of Medicine Prof. Dr. Ümmihan İşoğlu, Head of Child Health and Diseases Department of Nutrition and Metabolism Prof. Dr. Gülden Gökçay, Head of the Department of Child Health and Diseases, Prof. Dr. Zeynep Karakaş, Assoc. Fatmahan Atalar, Assoc. Asuman Gedikbaş, rarely international elites and many health sector members attended. Attention can be drawn to details on minor incidents that are rarely seen as an event that is practiced less than 1 in 2,000 at the ceremony. Plaque for Mukaddes and Ziya Karahan, the donors of the laboratory, and the breeder of the flower grower breeder.
5 million people in Turkey
It is stated that in Turkey, one out of 5 people rarely causes 70 of them in the classroom, 35 percent of the first-year deaths of children and 30 percent of the deaths before the age of 5 are caused by rarity. He travels on occasional childhood journeys, often in education, and sometimes visits long-term childhood doctors.
“There was a need for laboratories that were really hard to put in”
Tufan Tükek said, “Because it is general hereditary and genetically based, and is used as a technical basis for minor engineering processes, the dean of medicine, Prof. Dr., will be trained as the first person to start with. A normal life will be maintained. It may be for nearly 5 million sick patients, maybe more patients than this one. Such laboratories may be needed for early diagnosis, and such a laboratory may be sufficient for us to live in our faculty and in this situation for us. By studying their blood here, it will be revealed here whether it is a minor-based disease or not. Therefore, you continue to keep moving forward to talk about your goal to talk about the purpose of preventing this from a problem already in the absence of sight. It needs to be understood and thought through,” he said.
“80 of Rare child hunters”
In order to get detailed information about the rare tools in the society and the focus of attention of the educator, the head of the Nadalar Department of the Istanbul University Child Health Institute, Prof. Dr. It speaks of 7,000 years old. For him, with all this data, there is an accurate diagnosis and a lot too much.
“Encountering a life that we have never been able to meet with our life”
Stating that his daughter is also living with a rare disease, Deniz Yılmaz Atakay, the Founder of Rare Diseases, expressed the expression that sometimes the user name is rarely faced with. Atakay said, “Early diagnosis always saves lives. My daughter took Phenylketonuria patients, she came here on the 17th day, she was diagnosed on the 18th day, we encountered a life in which we were not told our name during the time. We aimed and taught her, our goal is to have a special diet for life and We encountered a life that we did not teach.