A Case Report of a Patient with Postpartum HELLP Syndrome
Background: HELLP syndrome is a multisystemic disorder characterized by elevated liver enzymes, hemolysis and low platelet count. If left untreated, it is associated with high risk of maternal and fetal mortality. It usually occurs in the third trimester
Maryam Moradi +2 more
doaj
Potentially pathogenic and pathogenic G6PD variants. [PDF]
Luzzatto L, Nannelli C, Notaro R.
europepmc +1 more source
Molecular Surveying of the Common Variants of Glucose 6-Phosphate Dehydrogenase Gene in Deficient Patients [PDF]
Glucose 6-phoshphate dehydrogenase is X-chromosome linked that expressed in all tissues. This is the first enzyme of pentose phosphate pathway were 5-carbon sugar Ribose and NADPH were synthesized by coupled oxidation /reduction reactions and this enzyme
doaj
At-Risk Genomic Findings for Pediatric-Onset Disorders From Genome Sequencing vs Medically Actionable Gene Panel in Proactive Screening of Newborns and Children. [PDF]
Balciuniene J +15 more
europepmc +1 more source
Glowing Spicules and Structural Collapse: A Single-Cell Insight into the Oxidative Aging of Favism Erythrocytes. [PDF]
Longo G, Dinarelli S, Girasole M.
europepmc +1 more source
Awareness, Knowledge, and Self-Reported Clinical Experiences Related to Glucose-6-Phosphate Dehydrogenase Deficiency in Sardinia (Italy): A Descriptive Cross-Sectional Survey. [PDF]
Serreli G +3 more
europepmc +1 more source
Two Cases of Methemoglobinemia Secondary to Favism in Pediatric Patients With Unknown Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency. [PDF]
Sawaftah MA +3 more
europepmc +1 more source
Co-occurrence of acute hemolytic anemia and methemoglobinemia in a 74-year-old female with G6PD deficiency: A case report. [PDF]
Chen B, Han Y.
europepmc +1 more source
The Clinical Utility of Whole-Exome Sequencing in the Prenatal Diagnosis of Fetal Skeletal Dysplasia. [PDF]
Mei Y +8 more
europepmc +1 more source

