Primary alveolar hypoventilation and XXXXY chromosopathy

Submitted: February 11, 2016
Accepted: February 11, 2016
Published: February 11, 2016
Abstract Views: 625
PDF: 434
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

The association of primary alveolar hypoventilation (PAH) and chromosomic diseases has not been described previously. A 19 year-old man with Fraccaro’s syndrome (XXXXY karyotype) was admitted to evaluate chronic hypercapnic respiratory failure, pulmonary arterial hypertension and cor pulmonale. PAH was diagnosed. As effective treatment, such as non-invasive positive pressure ventilation (NIPPV), is available for this disorder we should intensify the search for PAH in patients with chromosome disease.

Dimensions

Altmetric

PlumX Metrics

Downloads

Download data is not yet available.

Citations

How to Cite

Samolski, D., A. Antón, M. Mayos, M. Subirana, and R. Güell. 2016. “Primary Alveolar Hypoventilation and XXXXY Chromosopathy”. Monaldi Archives for Chest Disease 65 (3). https://doi.org/10.4081/monaldi.2006.564.

Similar Articles

<< < 42 43 44 45 46 47 48 49 50 51 > >> 

You may also start an advanced similarity search for this article.