Chest configuration in children and adolescents with infantile nephropathic cystinosis compared with other chronic kidney disease entities and its clinical determinants

BACKGROUND: Infantile nephropathic cystinosis (INC) is a systemic lysosomal storage disease causing intracellular cystine accumulation, resulting in renal Fanconi syndrome, progressive kidney disease (CKD), rickets, malnutrition, and myopathy. An INC-specific disproportionately diminished trunk leng...

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Detalles Bibliográficos
Autores principales: Müller, Sophia, Kluck, Rika, Jagodzinski, Celina, Brügelmann, Malina, Hohenfellner, Katharina, Büscher, Anja, Kemper, Markus J., Fröde, Kerstin, Oh, Jun, Billing, Heiko, Thumfart, Julia, Weber, Lutz T., Acham-Roschitz, Birgit, Arbeiter, Klaus, Tönshoff, Burkhard, Hagenberg, Martina, Pavičić, Leo, Haffner, Dieter, Zivicnjak, Miroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584709/
https://www.ncbi.nlm.nih.gov/pubmed/37415042
http://dx.doi.org/10.1007/s00467-023-06058-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584709/
https://www.ncbi.nlm.nih.gov/pubmed/37415042
http://dx.doi.org/10.1007/s00467-023-06058-x

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