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Severe persistent pulmonary hypertension of the newborn and dysmorphic features in neonate with a deletion involving TWIST1 and PHF14: a case report
BACKGROUND: Persistent pulmonary hypertension is a well-known disease of the newborn that in most cases responds well to treatment with nitric oxide and treatment of any underlying causes. Genetic causes of persistent pulmonary hypertension of the newborn are rare. The TWIST1 gene is involved in mor...
Autores principales: | Schinagl, Carina, Melum, Guro Reinholt, Rødningen, Olaug Kristin, Bjørgo, Kathrine, Andresen, Jannicke Hanne |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559830/ https://www.ncbi.nlm.nih.gov/pubmed/28814329 http://dx.doi.org/10.1186/s13256-017-1402-4 |
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