Failure to thrive as presentation in a patient with 22q11.2 microdeletion

BACKGROUND: Abnormalities of chromosome 22q11, including deletions and translocations, have been described in association with different birth defects and malformations occurring in many combinations and degrees of severity. CASE PRESENTATION: We describe the case of an 8 month-old infant with no dy...

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Detalles Bibliográficos
Autores principales: Bossi, Grazia, Gertosio, Chiara, Meazza, Cristina, Farello, Giovanni, Bozzola, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750288/
https://www.ncbi.nlm.nih.gov/pubmed/26864739
http://dx.doi.org/10.1186/s13052-016-0224-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750288/
https://www.ncbi.nlm.nih.gov/pubmed/26864739
http://dx.doi.org/10.1186/s13052-016-0224-0

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