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...

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Detalles Bibliográficos
Autores principales: Shankar, Vinay Hanyalu, Adithya-Sateesh, Bharadwaj, Gousy, Nicole, Ayele, Girma, Petursson, Freyr, Atalay, Rediet, Michael, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Case Report
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

Internet

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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