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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...
Autores principales: | Bossi, Grazia, Gertosio, Chiara, Meazza, Cristina, Farello, Giovanni, Bozzola, Mauro |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
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 |
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