H syndrome treated with Tocilizumab: two case reports and literature review

H syndrome is a rare autosomal recessive genetic disorder characterized by the following clinical features: cutaneous hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, short stature, hallux valgus, hyperglycemia, fixed flexion contractures of the toe...

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Detalles Bibliográficos
Autores principales: Jacquot, Robin, Jouret, Maurine, Valentin, Mathieu Gerfaud, Richard, Maël, Jamilloux, Yvan, Rousset, Florent, Emile, Jean-François, Haroche, Julien, Steinmüller, Lars, Zekre, Franck, Phan, Alice, Belot, Alexandre, Seve, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451072/
https://www.ncbi.nlm.nih.gov/pubmed/37638031
http://dx.doi.org/10.3389/fimmu.2023.1061182

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451072/
https://www.ncbi.nlm.nih.gov/pubmed/37638031
http://dx.doi.org/10.3389/fimmu.2023.1061182

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