Zobrazeno 1 - 10
of 193
pro vyhledávání: '"Microcytic hypochromic anemia"'
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 17, Iss 3 (2024)
Background: Iron deficiency anaemia (IDA) and thalassemia traits are the common conditions of microcytic hypochromic anaemia in pregnant women. However, the laboratory tests to differentiate them are expensive. The reticulocyte haemoglobin (Ret-Hb) t
Externí odkaz:
https://doaj.org/article/22030267f9a84e96b8aecbc9eb108504
Autor:
Muhammad Matloob Alam, Abdulrhman Alathaibi, Badriah Gharamah Alasmari, Mohammad Aljabri, Muhammad Kashif, Riffat Matloob, Mustafa Mohamed Selim
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 31, Iss 1, Pp 14-19 (2024)
Nabais Sa-de Vries syndrome (NSDVS) is a neurodevelopmental disorder first described in 2020. The syndrome is caused by de novo missense mutations in speckle-type pox virus and zinc finger protein (SPOP) on chromosome 17q21. In this report, we presen
Externí odkaz:
https://doaj.org/article/310f13e278a34e03a2b341bbe27c9681
Publikováno v:
GAIMS Journal of Medical Sciences, Vol 4, Iss 1, Pp 188-191 (2024)
Background Anemia represents a major healthcare burden in developing country like India. Since decades peripheral blood smear has been used for diagnosis of anemia. Cell counter has been introduced with increasing efficacy and a decreasing cost all
Externí odkaz:
https://doaj.org/article/3d4230e264d649e5ba81d73b55162e87
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 1, Pp 37-39 (2024)
Background: Hypotransferrinemia is a rare cause of anemia presenting in early childhood. The clinical scenario may mimic iron deficiency anemia at onset with no response to multiple courses of hematinics. Secondary complications may be due to iron ov
Externí odkaz:
https://doaj.org/article/4d2b35b5b6ee4cc0a92c312a663517df
Autor:
Xiuqin Bao, Jicheng Wang, Danqing Qin, Cuize Yao, Jie Liang, Kailing Liang, Yukun Zeng, Li Du
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-7 (2023)
Abstract Background At present, the methods generally used to detect α-thalassemia mutations are confined to detecting common mutations, which may lead to misdiagnosis or missed diagnosis. The single-molecule real-time (SMRT) sequencing enables long
Externí odkaz:
https://doaj.org/article/3a60b74a53f742b6b2ede8a19908c8db
Autor:
Umme Kulsoom Sheema, Alka Rawekar
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 11, Iss 6, Pp 2320-2326 (2022)
Iron-deficiency anemia (IDA) is a common nutritional disorder and an important risk factor for the development of mild cognitive impairment that may progress to dementia, if untreated. The anemic status due to iron deficiency (ID) alters the electrog
Externí odkaz:
https://doaj.org/article/97b065972f24448aac16a54517b328ce
Autor:
Saif Aboud M. Alqahtani
Publikováno v:
Clinics and Practice, Vol 11, Iss 3, Pp 494-504 (2021)
The thyroid gland plays a significant role in the metabolism and proliferation of blood cells; hematological disorders are frequently observed in patients with thyroid disorders, and the most frequent problem is anemia. The main objective of this res
Externí odkaz:
https://doaj.org/article/7e2719738a3343b2a60e58817eb8680f
Publikováno v:
Majalah Kedokteran Bandung, Vol 53, Iss 2, Pp 83-86 (2021)
In pregnant women there is a twofold increase in iron requirements due to increased blood volume without the expansion of plasma volume. Pregnant women are very prone to suffering from iron deficiency anemia. Iron deficiency anemia generally has an e
Externí odkaz:
https://doaj.org/article/8f8e04062304463780d2faa21bb13d6d
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Publikováno v:
Journal of Family Medicine and Primary Care, Vol 8, Iss 3, Pp 899-903 (2019)
Background: In developing world, anemia is a significant cause of mortality and morbidity in children under 5 years of age. Iron deficiency anemia (IDA) is a very important causative factor for childhood anemia. The aim of this study was to find the
Externí odkaz:
https://doaj.org/article/2b67f3f3877e4c4c9a9ded30da5b6d74