Zobrazeno 1 - 10
of 27 662
pro vyhledávání: '"Sickle-cell–disease"'
Autor:
Venance Emmanuel Mswelo, Kayiira Mubaraka, Yasa Mohamed, Peter Kyaligonza, Elias Joseph Xwatsal
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Background Sickle cell disease is a genetic disease with multisystem involvement. More than 300,000 children are born with sickle cell disease globally, with the majority of cases being in Sub-Saharan Africa. In Uganda, about 20,000 children
Externí odkaz:
https://doaj.org/article/611c072bb63e4d3e996cd6c6b7aa7c03
Autor:
Khaled Elzorkany, Mortadah Alsalman, Muthana AlSahlawi, Azam Alhedhod, Nasser Abdullah Almulhim, Nora Jalal Alsultan, Eman Mohammed Al-Ali, Eman Ali, Nawal Eltayeb Omer
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract Sickle cell disease (SCD) is the most common monogenic disorder in Saudi Arabia, which associates with an increased risk of organs damage, including the kidney. The aim of this study is to investigate the prevalence and predictors of sickle
Externí odkaz:
https://doaj.org/article/47c94106c9b84c71b2c1cc3b4e66ccc7
Autor:
Patre Vivek, Chandrakar Nobal
Publikováno v:
Journal of Ultrasonography, Vol 24, Iss 97, Pp 1-4 (2024)
To evaluate the pattern of renal artery Doppler indices in patients with sickle cell disease who do not have laboratory evidence of renal impairment.
Externí odkaz:
https://doaj.org/article/dc6277e55f3d4a8a842029ab9e582481
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Introduction Stroke is one of the most devastating complications of sickle cell disease (SCD). Transcranial Doppler Imaging (TCDI) is the least invasive screening method to predict patients at risk for developing stroke in the disease. After
Externí odkaz:
https://doaj.org/article/6e33a68533af4ef293979f5e559728c4
Publikováno v:
Egyptian Liver Journal, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Background Sickle cell hepatopathy (SCH) is a relatively uncommon complication of sickle cell disease (SCD), yet it does not accommodate variations in presentation, outcome, or severity according to age. Aim To present SCH characteristics an
Externí odkaz:
https://doaj.org/article/5983937427ca4007a032599aa8e59f58
Publikováno v:
eJHaem, Vol 5, Iss 5, Pp 920-928 (2024)
Abstract Sickle cell disease is a rare genetic disease resulting from an abnormality in hemoglobin. Hemostasis in the steady state, defined as ≥2 months without vaso‐occlusive crises, is poorly described in the literature. We report the routine h
Externí odkaz:
https://doaj.org/article/021e352dfdee44468b9fd57372b3693c
Autor:
Ramesh Khadayat, Mukesh Bishwakarma, Shubham Pant, Om Prakash Bhatta, Pariwesh Raj Bista, Sher Bahadur Kamar
Publikováno v:
eJHaem, Vol 5, Iss 5, Pp 913-919 (2024)
Abstract Background Sickle cell disease (SCD) is the most common hemoglobinopathy caused by an autosomal recessive genetic disorder leading to increased morbidity and mortality rates. SCD is prevalent in the Tharu community in the lowland (Terai) reg
Externí odkaz:
https://doaj.org/article/87a3bd6b11f846c49cd2c87e000fb281
Autor:
Rahma Menshawey, Esraa Menshawey
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-12 (2024)
Abstract Background Sickle cell disease (SCD) is the most common hemoglobinopathy worldwide, characterized by vaso-occlusive crises and ischemia that affects patients on a multi-system level. Despite being a genetically simple disease due to a single
Externí odkaz:
https://doaj.org/article/4b452427998b46e2949d2467283f5195
Autor:
Ilham Youssry, Abla S. Mostafa, Dina H. Hamed, Yasmin F. Abdel Hafez, Irene E. Bishai, Yasmeen M. M. Selim
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract Background Endothelial dysfunction is an integral pathophysiologic mechanism in sickle cell disease (SCD), and can lead to many complications. Sleep-disordered breathing (SDB) is a SCD complication with diverse incidence and pathophysiology.
Externí odkaz:
https://doaj.org/article/ac006e140c504e0db19dc13f359617f3
