Netherton Syndrome in a Neonate with Possible Growth Hormone Deficiency and Transient Hyperaldosteronism

Netherton syndrome, a rare autosomal recessive genetic disorder, is classified as an ichthyosiform syndrome. In this report we present the case of a neonate with erythroderma shortly after birth, accompanied by severe hypernatremia, recurrent infections, transient hyperaldosteronism, and signs of gr...

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Detalles Bibliográficos
Autores principales: Ilias, Chatziioannidis, Evgenia, Babatseva, Aikaterini, Patsatsi, Asimina, Galli-Tsinopoulou, Constantina, Sarri, Maria, Lithoxopoulou, George, Mitsiakos, Paraskevi, Karagianni, Christos, Tsakalidis, Zissis, Mamuris, Nikolaos, Nikolaidis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502330/
https://www.ncbi.nlm.nih.gov/pubmed/26229701
http://dx.doi.org/10.1155/2015/818961

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502330/
https://www.ncbi.nlm.nih.gov/pubmed/26229701
http://dx.doi.org/10.1155/2015/818961

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