Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maher R. Omair"'
Autor:
Naglaa M. Kamal, AlaaEddin M. Alzeky, Maher R. Omair, Ruwayd A. Attar, Abdullah M. Alotaibi, Abdullah Safar, Nawal S. Alosaimi, Sara A. S. Abosabie
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-6 (2022)
Abstract Background Myogenic Arthrogryposis Multiplex Congenita type 3 (AMC-3), is a rare congenital condition characterized by severe hypotonia, club feet, and multiple joint contractures often affecting both arms and legs which start prior to birth
Externí odkaz:
https://doaj.org/article/1b2ec14e732a499c9ca98b34bf91863b
Autor:
Abdullah Alotaibi, Maher R Omair, Alaaeddin Alzeky, Abdullah safar, Ruwayd Attar, Naglaa Kamal
Introduction: Arthrogryposis multiplex congenita (AMC), is a rare congenital condition characterized by multiple joint contractures often affecting both arms and legs which start prior to birth.Patient concern: The pediatrician attending delivery not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7282ee16cfa96f386513639e9b99f93
https://doi.org/10.21203/rs.3.rs-1053130/v1
https://doi.org/10.21203/rs.3.rs-1053130/v1
Autor:
Naglaa M. Kamal, AlaaEddin M. Alzeky, Maher R. Omair, Ruwayd A. Attar, Abdullah M. Alotaibi, Abdullah Safar, Nawal S. Alosaimi, Sara A. S. Abosabie
Publikováno v:
Italian journal of pediatrics. 48(1)
Background Myogenic Arthrogryposis Multiplex Congenita type 3 (AMC-3), is a rare congenital condition characterized by severe hypotonia, club feet, and multiple joint contractures often affecting both arms and legs which start prior to birth. Case pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55299161570d7d8b56faaef7f35e9549
https://pubmed.ncbi.nlm.nih.gov/35739559
https://pubmed.ncbi.nlm.nih.gov/35739559