Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose-6-phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm

MeSH terms

• Anemia / diagnosis
• Anemia / genetics*
• Dominican Republic
• Elliptocytosis, Hereditary / genetics*
• Family Health
• Female
• Glucosephosphate Dehydrogenase / genetics*
• High-Throughput Nucleotide Sequencing / methods
• Humans
• Infant, Newborn
• Inheritance Patterns / genetics
• Male
• Mutation*
• Pyruvate Kinase / genetics*
• Rare Diseases / diagnosis
• Rare Diseases / genetics
• Twins, Monozygotic / genetics