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Autor:
Diar S. Hama-Karim, MD, Yad N. Othman, MBCHB, Zryan Salar Majeed, MBCHB, Razhan K. Ali, MBCHB, Arian Mohammed, MBCHB, Han Nihad Muhamad, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 3, Pp 1337-1341 (2023)
Homocystinuria is a rare genetic disease with autosomal recessive pattern. It is reported to be highest in Arabian descend and could cause thrombosis, but mainly peripherally. Cardiac amorphous tumor has been recognized in the past 20 years and it is
Externí odkaz:
https://doaj.org/article/b0c3e15e591849f38cbd241eabd7cc03