Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Hemoglobin C trait"'
Autor:
Xavier Garrell-Salat, Claudia Garcia-Arumi, Yann Bertolani, Sandra Banderas García, Paul Buck, Jose Garcia-Arumi
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 53, Iss 5, Pp 318-321 (2023)
Hemoglobin C (HbC) disease is an uncommon disease that is generally considered benign, causing only occasionally painless hematuria, osteomyelitis, and dental abnormalities. Ocular manifestations have rarely been described in these patients. Here we
Externí odkaz:
https://doaj.org/article/605dee1fb4ec4ea586084107a0f17c24
Akademický článek
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Akademický článek
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Autor:
Sara M. Briker, Jessica Y. Aduwo, Regine Mugeni, Margrethe F. Horlyck-Romanovsky, Christopher Dubose, Anne E. Sumner
Publikováno v:
Diabetes. 68
Hemoglobin C (HbC) trait is a heterozygous hemoglobinopathy common in West Africa. Due to interference with the HPLC assay, heterozygous hemoglobinopathies such as HbC trait may lead to readings for A1C which are artefactually low. Therefore, the val
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d988343fbbf7182e6b4c2c43509586b6
https://doi.org/10.2337/db19-1494-p
https://doi.org/10.2337/db19-1494-p
Autor:
Jessica Y. Aduwo, Anne E. Sumner, Lilian Mabundo, Sara M. Briker, Christopher Dubose, Stephanie T. Chung, Margrethe F. Horlyck-Romanovsky, Regine Mugeni, Joon Ha, Arthur Sherman
Publikováno v:
Diabetes. 68
A1C is easier to perform than an OGTT, but A1C has a lower rate of detection of diabetes (DM) and prediabetes (preDM). Underperformance of A1C in the detection of hyperglycemia may be magnified in Africans. Three single gene mutations common in Afric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7f405da208e251a70341eba1c0ce98d
https://doi.org/10.2337/db19-1493-p
https://doi.org/10.2337/db19-1493-p
Publikováno v:
AACE Clinical Case Reports, Vol 5, Iss 1, Pp e31-e34 (2019)
Objective: Hemoglobin A1c (HbA1c) is a useful tool for the diagnosis and management of diabetes mellitus and generally an excellent marker of overall glycemic control for the preceding 8 to 12 weeks; however, the test is not without its pitfalls. A s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76dd0250fe5f51960d5ae2e7ca482caf
https://europepmc.org/articles/PMC6876969/
https://europepmc.org/articles/PMC6876969/
Akademický článek
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Publikováno v:
Pediatric Nephrology. 24:2455-2457
Patients with sickle cell disease commonly experience painless hematuria. Hematuria may be found in patients with sickle cell trait, sickle cell anemia, and sickle cell hemoglobin C disease, but it is believed to be uncommon in patients with other he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfe59146b99ded5ef5d6bbfa0769f9c6
https://doi.org/10.1007/s00467-009-1263-1
https://doi.org/10.1007/s00467-009-1263-1
Autor:
Erin B. Voelkel, Elizabeth Yang, Patrick G. Gallagher, Kimberly Lezon-Geyda, Vincent P. Schulz
Publikováno v:
Pediatric Blood & Cancer. 64:e26444
A 17-year-old male presented with acute hemolysis with stomatocytosis, elevated mean corpuscular hemoglobin concentration (MCHC), and osmotic gradient ektacytometry consistent with marked erythrocyte dehydration. Erythrocytes from both parents also d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c07bc4728a4616df9511b2b58a9a18a6
https://doi.org/10.1002/pbc.26444
https://doi.org/10.1002/pbc.26444
Autor:
Abdullah Sakarcan, James Stallworth
Publikováno v:
Pediatric Nephrology. 16:145-147
Hematuria is a rare complication seen in patients with hemoglobin C trait. We report a 15-year-old African-American female with hemoglobin C trait, who presented with persistent hematuria. None of the urological, serological or histological workups r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305f8a5ef607a2676b63cc94d045b314
https://doi.org/10.1007/s004670000532
https://doi.org/10.1007/s004670000532