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pro vyhledávání: '"Anas Alshorman"'
Autor:
Wafaa N. Al Rawi, Wala'a Al‐Safi, Ashraf N. Abuobayda, Nabil S. Elmansoury, Abhijeet S. Lonikar, Anas Alshorman, Hasansaheb D. Maldar
Publikováno v:
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract 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 trea
Externí odkaz:
https://doaj.org/article/0258f4fbf37241fe956c7970436cf6fb
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
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