Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report

BACKGROUND: Previous reports of chromosomal aberrations in different forms of congenital diaphragmatic hernia have been described as comprising aneuploidies (for example, trisomy 21), microdeletions, and duplications (for example, monosomy 15q24, 22q11.2). CASE PRESENTATION: We describe the first as...

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Detalles Bibliográficos
Autores principales: Bogs, Thomas, Kipfmüller, Florian, Kohlschmidt, Nicolai, Gembruch, Ulrich, Müller, Andreas, Reutter, Heiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818464/
https://www.ncbi.nlm.nih.gov/pubmed/27036947
http://dx.doi.org/10.1186/s13256-016-0855-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818464/
https://www.ncbi.nlm.nih.gov/pubmed/27036947
http://dx.doi.org/10.1186/s13256-016-0855-1

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