Hereditary orotic aciduria identified by newborn screening

Introduction: Hereditary orotic aciduria is an extremely rare, autosomal recessive disease caused by deficiency of uridine monophosphate synthase. Untreated, affected individuals may develop refractory megaloblastic anemia, neurodevelopmental disabilities, and crystalluria. Newborn screening has the...

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Detalles Bibliográficos
Autores principales: Staretz-Chacham, Orna, Damseh, Nadirah S., Daas, Suha, Abu Salah, Nasser, Anikster, Yair, Barel, Ortal, Dumin, Elena, Fattal-Valevski, Aviva, Falik-Zaccai, Tzipora C., Hershkovitz, Eli, Josefsberg, Sagi, Landau, Yuval, Lerman-Sagie, Tally, Mandel, Hanna, Rock, Rachel, Rostami, Nira, Saraf-Levy, Talya, Shaul Lotan, Nava, Spiegel, Ronen, Tal, Galit, Ulanovsky, Igor, Wilnai, Yael, Korman, Stanley H., Almashanu, Shlomo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043439/
https://www.ncbi.nlm.nih.gov/pubmed/36999056
http://dx.doi.org/10.3389/fgene.2023.1135267

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043439/
https://www.ncbi.nlm.nih.gov/pubmed/36999056
http://dx.doi.org/10.3389/fgene.2023.1135267

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