Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mahmud, Elfituri"'
Autor:
Murad Almasri, Kamleshun Ramphul, Mahmud Elfituri, Rashmitha Dachepally, Petras Lohana, Renuka Verma, Shaheen Sombans, Balkiranjit Kaur Dhillon
Publikováno v:
Heart Rhythm. 20:S681
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6879e746d83a129b6d6dfba4754de45b
https://doi.org/10.1016/j.hrthm.2023.03.1420
https://doi.org/10.1016/j.hrthm.2023.03.1420
Publikováno v:
Cureus
This case report details the clinical course of a 7-year-old patient with an initial presentation of acute appendicitis, who developed symptoms highly concerning multisystem inflammatory syndrome in children (MIS-C) after appendectomy. Despite approp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53a007ce5e9a2c2f6a6d8adff1124de2
https://doi.org/10.7759/cureus.17084
https://doi.org/10.7759/cureus.17084
Autor:
Rehab, Ali, Nader, Al-Dewik, Shayma, Mohammed, Mahmud, Elfituri, Sahar, Agouba, Sara, Musa, Laila, Mahmoud, Mariam, Almulla, Karen, El-Akouri, Howaida, Mohd, Reem, Bux, Hajer, Almulla, Amna, Othman, Fatma, Al-Mesaifri, Noora, Shahbeck, Mariam, Al-Muriekhi, Amal, Khalifa, Reem, Al-Sulaiman, Tawfeg, Ben-Omran
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 188(1)
Woodhouse-Sakati syndrome (WSS) is a rare autosomal recessive neuroendocrine and ectodermal disorder caused by variants in the DCAF17 gene. In Qatar, the c.436delC variant has been reported as a possible founder pathogenic variant with striking pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c72a362d84a8076c7051cfd88014dde
https://pubmed.ncbi.nlm.nih.gov/34590781
https://pubmed.ncbi.nlm.nih.gov/34590781