A rare case of Allgrove Syndrome associated with growth hormone deficiency in an 8-year-Old child: A case report

INTRODUCTION AND IMPORTANCE: Triple A (Allgrove) syndrome is an autosomal recessive multi-organ disease, caused by a mutated gene on chromosome 12q13 in most cases, characterized by the classic triad of Alacrimia, Achalasia and Adrenal insufficiency; along with neurologic abnormalities and many othe...

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Detalles Bibliográficos
Autores principales: Eid, Mahfoud, Chreitah, Ahmad, Aljanati, Omar, Mohammed, Aria, Melhem, Ibrahim, Alkilany, Zeina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486606/
https://www.ncbi.nlm.nih.gov/pubmed/36147172
http://dx.doi.org/10.1016/j.amsu.2022.104352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486606/
https://www.ncbi.nlm.nih.gov/pubmed/36147172
http://dx.doi.org/10.1016/j.amsu.2022.104352

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