Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Hemoglobin Barts"'
Publikováno v:
Journal of Ultrasound in Medicine. 40:659-674
Insights gained from this review are as follows: (1) Ultrasound is highly effective in early detection of fetal hemoglobin (Hb) Bart disease. (2) The most sensitive parameters in predicting Hb Bart anemia appear to be the cardiac diameter-to-thoracic
Publikováno v:
Open Access Macedonian Journal of Medical Sciences, Vol 8, Iss E (2020)
Open Access Macedonian Journal of Medical Sciences; Vol. 8 No. E (2020): E-Public Health; 236-240
Open Access Macedonian Journal of Medical Sciences; Vol. 8 No. E (2020): E-Public Health; 236-240
BACKGROUND: Alpha-thalassemia is a major health problem for worldwide populations due to its recent large-scale global movements to many other parts of the world. The most effective method to prevent the spread of the worst form of α-thalassemia dis
Autor:
Mark Curran, Wang-Dar Sun, Ramen H. Chmait, Anna Leung, Gira Morchi, Michel Mikhael, Jina Lim
Publikováno v:
AJP Reports
American Journal of Perinatology Reports, Vol 10, Iss 01, Pp e11-e14 (2020)
American Journal of Perinatology Reports, Vol 10, Iss 01, Pp e11-e14 (2020)
We describe a fetus at 24 3/7 weeks' gestation that showed ultrasound evidence of anemia, hydrops, and severe growth restriction. Both parents were known to be cis heterozygous carriers for SEA α-thalassemia deletion (αα/–). Cordocentesis confir
Autor:
Pamela P. W. Lee, Godfrey Chi-Fung Chan, Wilson Yau-Ki Chan, Vincent Lee, Wing Leung, Daniel Ka Leung Cheuk, Shau-Yin Ha
Publikováno v:
Pediatric transplantationREFERENCES. 25(6)
Background Hemoglobin Bart's hydrops fetalis syndrome (BHFS) was once considered a fatal condition universally. Medical advances over the past three decades have resulted in increasing numbers of BHFS survivors. This retrospective review summarized l
Akademický článek
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Autor:
Brandi Bell-Carey, Rupsa C. Boelig, Dana Neumann, Margaret A. Lafferty, Rose Guo, Caroline Edwards, Richard J. Derman, Jay S. Greenspan, Zubair H. Aghai
Publikováno v:
The Journal of pediatrics. 227
To determine the prevalence of low mean corpuscular volume (MCV) in newborn infants admitted to the neonatal intensive care unit and to assess low MCV as a diagnostic test for alpha thalassemia.Retrospective analysis of all infants admitted to the ne
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in MedicineReferences. 40(3)
Objectives To evaluate the efficacy of the fetal heart diameter (HD) in predicting fetal hemoglobin (Hb) Bart disease at midpregnancy. Methods Video clips of fetal chest ultrasound examinations performed on fetuses at risk of Hb Bart disease at 18 to
Publikováno v:
Pediatric and Developmental Pathology. 22:166-170
Alpha thalassemia major is a hemoglobinopathy caused by the inactivation or deletion of all 4 α-globin alleles. We describe a case of α-thalassemia major with atypical ultrasound and neuropathological findings. The mother had her first prenatal vis
Publikováno v:
Pediatric and Developmental Pathology. 20:298-307
The pulmonary neuroendocrine system includes pulmonary neuroendocrine cells (PNECs) and neuroepithelial bodies (NEBs) that are distributed throughout respiratory epithelium and regulate lung growth and maturation antenatally. Abnormalities in this sy
Autor:
Sakorn Pornpresert, Matawee Pongpaiboon, Supansa Pata, Kittiphong Paiboonsukwong, Suthat Fucharoen, Thongperm Munkongdee, Watchara Kasinrerk, Witida Laopajon
Publikováno v:
Biological Procedures
Background Couples who carry α-thalassemia-1 deletion are at 25% risk of having a fetus with hemoglobin Bart’s hydrops fetalis. Southeast Asian deletion (−-(SEA)) is the most common type of α-thalassemia 1 among Southeast Asian populations. Thu