Literature DB >> 7617602

[Clinical late manifestation of Ondine's syndrome with pronounced primary, especially sleep related alveolar hypoventilation].

J Schlegel1, K Kienast, B Fischer, R Ferlinz.   

Abstract

We report on a very rare case of a primary, alveolar hypoventilation syndrome (Ondine's Curse syndrome) in a female patient who was first treated at the age of 26 years as a result of an influenza infection; however, the case history revealed a decreased performance in comparison to similar aged children from earliest childhood onwards as well as an intermittent zyanosis of the lips and distal extremities. Other diseases which could explain a global respiratory insufficiency and/or pulmonary arterial hypertension were excluded.

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Mesh:

Year:  1995        PMID: 7617602

Source DB:  PubMed          Journal:  Pneumologie        ISSN: 0934-8387


  2 in total

1.  Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report.

Authors:  Lia Rita Azeredo Bittencourt; Mario Pedrazzoli; Fabiana Yagihara; Gabriela Pontes Luz; Silvério Garbuio; Gustavo Antonio Moreira; João Aléssio J Perfeito; Sergio Tufik
Journal:  Sleep Breath       Date:  2011-11-19       Impact factor: 2.816

2.  Congenital central hypoventilation syndrome (Ondine's curse syndrome) in two siblings: delayed diagnosis and successful noninvasive treatment.

Authors:  R Kerbl; H Litscher; H M Grubbauer; F Reiterer; G Zobel; M Trop; B Urlesberger; E Eber; R Kurz
Journal:  Eur J Pediatr       Date:  1996-11       Impact factor: 3.183

  2 in total

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