Secondary Hyperparathyroidism in Children with Mucolipidosis Type II (I-Cell Disease): Irish Experience

Mucolipidosis type II (ML II) is an autosomal recessive lysosomal targeting disorder that may present with features of hyperparathyroidism. The aim of this study was to describe in detail the clinical cases of ML II presenting to a tertiary referral centre with biochemical and/or radiological featur...

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Detalles Bibliográficos
Autores principales: Boruah, Ritma, Monavari, Ahmad Ardeshir, Conlon, Tracey, Murphy, Nuala, Stroiescu, Andreea, Ryan, Stephanie, Hughes, Joanne, Knerr, Ina, McDonnell, Ciara, Crushell, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911139/
https://www.ncbi.nlm.nih.gov/pubmed/35268460
http://dx.doi.org/10.3390/jcm11051366

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911139/
https://www.ncbi.nlm.nih.gov/pubmed/35268460
http://dx.doi.org/10.3390/jcm11051366

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