Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ashraf Abuobayda"'
Autor:
Wafaa Alrawi, Taisser Atrak, Ashraf Abuobayda, Nabil Elmansoury, Omer Elnakeib, Abhijeet Lonikar
Infants born at 22–23 weeks rarely survive, and most develop severe complications, especially in the case of multiple births. This age is considered the threshold for active intervention. We report the survival of twins born at 22 2/7 weeks gestati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25acd48b336e01debfdf2b411aeb33cf
https://doi.org/10.22541/au.165854522.21703265/v1
https://doi.org/10.22541/au.165854522.21703265/v1
Autor:
Wafaa Alrawi, Taisser Atrak, Ashraf Abuobayda, Nabil Elmansoury, Omar Elnakeib, Abhijeet Lonikar
Publikováno v:
Medicine. 102:e32571
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14cb75a122f1598f8a366c4e231cda70
https://doi.org/10.1097/md.0000000000032571
https://doi.org/10.1097/md.0000000000032571
Autor:
Wala'a Al‐Safi, Anas Alshorman, Nabil S. Elmansoury, Abhijeet S. Lonikar, Hasansaheb D. Maldar, Ashraf Abuobayda, Wafaa N. Al Rawi
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Our findings expand the known clinical features of trisomy 13 by including ectrodactyly as a possible Trisomy 13‐associated limb malformation. We highlight the importance of performing antenatal genetic test to establish more specific treatment pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::828c1a1e654b7ba5c4ea83c3baa09083
http://europepmc.org/articles/PMC8144878
http://europepmc.org/articles/PMC8144878
Autor:
Abhijeet S. Lonikar, Nabil S. Elmansoury, Wafaa Alrawi, Anas Alshorman, Hasansaheb D. Maldar, Ashraf Abuobayda
In 2020, we had reported one of the few cases of trisomy 13 with ectrodactyly, a rare form of limb deformity. Herein, we report another newborn who suffered from trisomy 13 and ectrodactyly. The patient also possessed another unusual manifestation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56a90a7e5fe7f8d25dd3b42b02252416
https://doi.org/10.22541/au.161371897.76133900/v1
https://doi.org/10.22541/au.161371897.76133900/v1
Publikováno v:
Journal of Clinical Neonatology. 9:143
Trisomy 13 (Patau syndrome) is third common trisomy and associated with multiple congenital anomalies including limb malformation like polydactyly. However, the presence of ectrodactyly or split-hand and/or foot malformation, a lobster claw-like appe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa9bdedbacc598fcc2a72559480d62fe
https://doi.org/10.4103/jcn.jcn_130_16
https://doi.org/10.4103/jcn.jcn_130_16