Premature Loss of Permanent Teeth in Allgrove (4A) Syndrome in Two Related Families

BACKGROUND: Allgrove syndrome is a rare autosomal recessive condition characterized by adrenal insufficiency, achalasia, alacrima and occasionally autonomic disturbances. Mutations in the AAAS gene, on chromosome 12q13 have been implicated as a cause of this disorder. CASE(S) PRESENTATION: We presen...

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Detalles Bibliográficos
Autores principales: Razavi, Zahra, Taghdiri, Mohammad-Mehdi, Eghbalian, Fatemeh, Bazzazi, Nooshin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446014/
https://www.ncbi.nlm.nih.gov/pubmed/23056690

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446014/
https://www.ncbi.nlm.nih.gov/pubmed/23056690

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