Oral health care knowledge among Phenylketonuria patients in the Latvian population
Background: Phenylketonuria (PKU) is an autosomal recessive inherited disorder of phenylalanine (Phe) metabolism that results from a deficiency of phenylalanine hydroxylase (PAH). Patients with PKU rely on amino acid mixtures and low-protein diets, which often exhibit an acidic nature and pose vario...
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| Main Authors: | Iveta Abola, Nikola Anna Intlere, Anda Brinkmane, Sabine Laktina, Agnese Zarina, Lauma Vasilevska, Ingus Skadins, Georgijs Moisejevs, Linda Gailite, Madara Auzenbaha |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-12-01
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| Series: | Molecular Genetics and Metabolism Reports |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2214426924001204 |
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