Clinical overview and outcome of the Stuve-Wiedemann syndrome: a systematic review

BACKGROUND: Stuve-Wiedemann syndrome (SWS) is a rare and severe genetic disease characterized by skeletal anomalies and dysautonomic disturbances requiring appropriate care. Peer support is mandatory to fill the lack of clinical recommendations in such rare diseases. We report a new case and provide...

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Detalles Bibliográficos
Autores principales: Warnier, Hélène, Barrea, Christophe, Bethlen, Sarah, Schrouff, Isabelle, Harvengt, Julie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034487/
https://www.ncbi.nlm.nih.gov/pubmed/35461249
http://dx.doi.org/10.1186/s13023-022-02323-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034487/
https://www.ncbi.nlm.nih.gov/pubmed/35461249
http://dx.doi.org/10.1186/s13023-022-02323-8

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