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Homocystinuria patient and caregiver survey: experiences of diagnosis and patient satisfaction

BACKGROUND: The main genetic causes of homocystinuria are cystathionine beta-synthase (CBS) deficiency and the remethylation defects. Many patients present in childhood but milder forms may present later in life. Some countries have newborn screening programs for the homocystinurias but these do not...

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Bibliographische Detailangaben
Veröffentlicht in:Orphanet J Rare Dis
Hauptverfasser: Morrison, T., Bösch, F., Landolt, M. A., Kožich, V., Huemer, M., Morris, A. A. M.
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2021
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7945666/
https://ncbi.nlm.nih.gov/pubmed/33691747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-021-01764-x
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