Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Raniah S. Alotibi"'
Autor:
Mariam M. Al Eissa, Fahad Almsned, Reem R. Alkharji, Yousif M. Aldossary, Raghad AlQurashi, Esraa A. Hawsa, Sahar M. AlDosari, Amerh S. Alqahtani, Raniah S. Alotibi, Raed Farzan, Reema Alduaiji, Suha M. Sulimani, Shaker A. Alomary, Abdullah M. Assiri
Publikováno v:
BMC Public Health, Vol 24, Iss 1, Pp 1-15 (2024)
Abstract The prevalence of consanguineous marriages (CMs) varies worldwide from one country to another. However, the Middle East stands out as a region with a notably high rate of CMs. CM is particularly widespread in Saudi Arabia, where the prevalen
Externí odkaz:
https://doaj.org/article/e075f9b53e1d4562a0ab97292e5398a4
Autor:
Mariam M. Al Eissa, Raniah S. Alotibi, Bader Alhaddad, Taghrid Aloraini, Manar S. Samman, Abdulrahman AlAsiri, Mohamed Abouelhoda, Amerh S. AlQahtani
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Physicians face diagnostic dilemmas upon reports indicating disease variants of unknown significance (VUS). The most puzzling cases are patients with rare diseases, where finding another matched genotype and phenotype to associate their
Externí odkaz:
https://doaj.org/article/95ac75cb26ba4c4f8cf5594da067c504
Autor:
Amerh S. Alqahtani, Raniah S. Alotibi, Taghrid Aloraini, Fahad Almsned, Yara Alassali, Ahmed Alfares, Bader Alhaddad, Mariam M. Al Eissa
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Rare diseases (RDs) create a massive burden for governments and families because sufferers of these diseases are required to undergo long-term treatment or rehabilitation to maintain a normal life. In Saudi Arabia (SA), the prevalence o
Externí odkaz:
https://doaj.org/article/a833fb18a8b94d34b8880c29e369f3f4
Autor:
Raniah S. Alotibi, Naif S. Sannan, Mariam AlEissa, Marwh G. Aldriwesh, Abeer Al Tuwaijri, Maaged A. Akiel, Mashael Almutairi, Alhanouf Alsamer, Nouf Altharawi, Ghadah Aljawfan, Badi Alotiabi, Mohammed A. AlBlawi, Ahmed Alfares
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundNeurodevelopmental disorders are a group of conditions characterized by developmental delays leading to abnormal brain functions. The methods of diagnosis and treatment of these conditions are complicated, and their treatment involves a com
Externí odkaz:
https://doaj.org/article/d00ea30db7dd4a65928be8f0a12d717f
Autor:
Fazal Hussain, Mohieldin Elsayid, Fahad Almohareb, Naif M. Alhawiti, Bdoor Alamri, Shoeb Qureshi, Eman Alharbi, Cherry Colcol, Bushra Aljuhani, Raniah S Alotibi
Publikováno v:
Journal of Natural Science, Biology and Medicine. 10:97
Background: β-thalassemia is an autosomal disorder of the blood caused by mutations in HBB gene responsible for the production of β-globin. The HBB mutations reduce the synthesis of β-globin which results in severe anemia. A high frequency of β-t