22q11 Deletion Syndrome and Urogenital Manifestations: A Clinicopathological Case Report

BACKGROUND: Deletion in the chromosomal region 22q11 results from the abnormal development of the third and fourth pharyngeal pouches during embryonic life and presents an expansive phenotype with more than 180 clinical features described that involve every organ and system. HISTORY AND SIGNS: A 23-...

Descripción completa

Detalles Bibliográficos
Autores principales: Vachette, M., Grant, G. E., Bouquet de la Joliniere, J., Jotterand, M., Ben Ali, N., Feki, A., Capoccia Brugger, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124728/
https://www.ncbi.nlm.nih.gov/pubmed/27965957
http://dx.doi.org/10.3389/fmed.2016.00053

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124728/
https://www.ncbi.nlm.nih.gov/pubmed/27965957
http://dx.doi.org/10.3389/fmed.2016.00053

Ejemplares similares