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Pyruvate Kinase Deficiency Causing Priapism
Pyruvate kinase deficiency (PKD) is an autosomal recessive defect of the enzyme pyruvate kinase (PK) which is involved in catalyzing a reaction that produces ATP in the glycolytic pathway. It is the most common defect of the glycolytic pathway associated with congenital anemia. Patients usually pres...
Autores principales: | Shankar, Vinay Hanyalu, Adithya-Sateesh, Bharadwaj, Gousy, Nicole, Ayele, Girma, Petursson, Freyr, Atalay, Rediet, Michael, Miriam |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185413/ https://www.ncbi.nlm.nih.gov/pubmed/37197195 http://dx.doi.org/10.1155/2023/6503311 |
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