Patients with the genotype of β/β for β-thalassemia (β-thal) usually behave as β-thal major (β-TM) phenotype which is transfusion-dependent. The pathophysiology of β-thal is the imbalance between α/β-globin chains. The degree of α/β-globin imbalance can be reduced by the more effective synthesis of γ-globin chains, and increased Hb F levels, modifying clinical severity of β-TM.
View Article and Find Full Text PDFHb Zürich-Albisrieden, [α59(E8)Gly→Arg, : c.178G>C] is a rare and highly unstable α-globin chain variant. The involved mutation has been reported in both and genes.
View Article and Find Full Text PDFWe report a new hemoglobin (Hb) variant that we have named Hb Wanjiang (: c.255_264delinsTTTTTCTCAG). We identified this variant in a Chinese man by the next-generation sequencing (NGS) method.
View Article and Find Full Text PDFObjectives: To develop a nomogram to predict the likelihood of vaginal birth after caesarean section (VBAC) among women after a previous caesarean section (CS).
Design: A retrospective cohort study.
Setting: Two secondary hospitals in Guangdong Province, China.
This retrospective analysis was set to understand the epidemiological status of the critically ill obstetric patients in Dongguan city, Guangdong, China. Understanding the risk factors for the death cases can provide scientific evidences for future preventive strategies to decrease the maternal mortality rate. This retrospective included the statistical data and clinical data on the cases of critically ill and dead obstetric patients admitted to Dongguan People's Hospital and Dongguan Maternal & Child Health Hospital from September 1st, 2009 to August 31st, 2013.
View Article and Find Full Text PDF