Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Samuel Sisay Hailu, MD"'
Autor:
Desalegn Fekadu, MD, Suleyman Fantahun, MD, Abdi Alemayehu, MD, Yohannes Eshetu, MD, Gemechis Assefa, MD, Samuel Sisay Hailu, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4675-4681 (2024)
Right-sided aortic arch, first documented by Fioratti and Aglietti in 1763, is a rare variant of the thoracic vascular anatomy present in about 0.1% of the adult population. In half of these cases the left subclavian artery is also aberrant. The aber
Externí odkaz:
https://doaj.org/article/bfdc93119b2c481a8328bed6665c3b74
Autor:
Michael Teklehaimanot Abera, MD, Misganaw Badege Fetene, MD, Nibretu Bekele Kassa, MD, Yodit Abraham Yaynishet, MD, Tesfaye Gizaw Tefera, MD, Samuel Sisay Hailu, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 5, Pp 1949-1955 (2024)
Tuberculosis is one of the most common pediatric problems, especially in the developing world. In spite of that, intraocular tuberculosis is a rare disease that can easily be confused with other noninfectious processes, even in regions where tubercul
Externí odkaz:
https://doaj.org/article/dccf9c2773cb49e0966913bc14bdb9e9
Publikováno v:
Radiology Case Reports, Vol 19, Iss 4, Pp 1496-1502 (2024)
Congenital lobar overinflation is a rare but well-recognized congenital cause of neonatal and infantile respiratory distress. At times, the condition can mimic other congenital or acquired diseases and have atypical distribution and imaging patterns.
Externí odkaz:
https://doaj.org/article/cfc18b2472844b66aa131c3b50b74620
Autor:
Raja Tamiru, MD, Tesfahunegn Hailemariam, MD, Amanuel Aboye, MD, Bethel Germamo, MD, Yodit Abraham, MD, Erko Chala, MD, Samuel Sisay Hailu, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 2, Pp 727-731 (2024)
Jarcho-Levin syndrome (JLS) is a congenital dysostosis characterized by multiple vertebral and intrinsic rib abnormalities. JLS and neural tube abnormalities rarely occur together. There have been few cases of JLS associated with a split spinal cord
Externí odkaz:
https://doaj.org/article/45b36db9e4334c40a35019d8e3cd129d
Publikováno v:
Radiology Case Reports, Vol 18, Iss 10, Pp 3376-3379 (2023)
Generalized arterial calcification of infancy (GACI) is a rare condition characterized by diffuse arterial calcification within the internal elastic lamina associated with intimal proliferation leading to stenosis of great and medium-sized vessels, w
Externí odkaz:
https://doaj.org/article/d32604bd17804439b58adb0625ac8496
Publikováno v:
Radiology Case Reports, Vol 18, Iss 9, Pp 2966-2970 (2023)
Beckwith-Wiedemann syndrome (BWS) is a rare imprinting disorder and overgrowth syndrome with a prevalence of 1 in 10,000 live births. It is characterized by predilection for embryonal tumor growth, especially Wilms tumor (WT), and manifestations like
Externí odkaz:
https://doaj.org/article/e95fe6246dea4e039652df94191dcb17
Autor:
Samuel Sisay Hailu, MD, SRAD, SSPRAD, Daniel Zewdneh Solomon, MD, SRAD, SSPRAD, MHA, HDP, Yocabel Gorfu Gebremedhin, MD, SRAD, SSPRAD, HDP, Amal Saleh Nour, MD, SRAD, SSNEURORAD, HDP
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3820-3824 (2022)
A parasitic or heteropagus twin is a grossly defective fetus (or fetus part) attached externally, with or without internal connections and is dependent on the cardiovascular system of the other twin (autosite) for survival. The estimated incidence is
Externí odkaz:
https://doaj.org/article/9e70f6b6d2ff4d31b46c56577e8c1e6f