Supportive care in a patient with Alstrom syndrome with hyperphenylalaninemia and sleep problems

Alstrom syndrome is a rare genetic disorder with an autosomal recessive mutation in the ALMS1 gene. The disease's manifestations include ophthalmic problems, hearing loss, obesity, and cardiovascular disorders. In addition, medical cases include other organ complications. However, the overlappi...

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Detalles Bibliográficos
Autores principales: Jalilolghadr, Shabnam, Saffari, Fatemeh, Alizadeh, Mehdi, Taremiha, AliReza, Ghodsi, Marjan, Ghodsi, Mersedeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900236/
https://www.ncbi.nlm.nih.gov/pubmed/36777792
http://dx.doi.org/10.1002/ccr3.6894

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900236/
https://www.ncbi.nlm.nih.gov/pubmed/36777792
http://dx.doi.org/10.1002/ccr3.6894

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