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21 Σεπ 2020 · Congenital Central Hypoventilation Syndrome (CCHS) is a rare condition characterized by an alveolar hypoventilation due to a deficient autonomic central control of ventilation and a global autonomic dysfunction. Paired-like homeobox 2B (PHOX2B) mutations are found in most of the patients with CCHS.
- Table - PMC - National Center for Biotechnology Information
Congenital Central Hypoventilation Syndrome (CCHS) is a rare...
- Role of calretinin immunohistochemical stain in evaluation of ...
Introduction. Hirschsprung’s disease is a congenital defect...
- Congenital central hypoventilation syndrome: diagnostic and management ...
Congenital central hypoventilation syndrome (CCHS) is a rare...
- Congenital Central Hypoventilation Syndrome - GeneReviews® - NCBI Bookshelf
Congenital central hypoventilation syndrome (CCHS)...
- Table - PMC - National Center for Biotechnology Information
18 Αυγ 2016 · Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder of the autonomic nervous system (ANS) due to a mutation in the paired-like homeobox 2B (PHOX2B) gene. 1 CCHS patients usually present in the newborn period with apnea, hypoxemia, and hypercapnia without clinical signs of respiratory compromise that occur and are most ...
28 Ιαν 2004 · Congenital central hypoventilation syndrome (CCHS) represents the extreme manifestation of autonomic nervous system dysregulation (ANSD) with the hallmark of disordered respiratory control.
14 Μαρ 2023 · Congenital central hypoventilation syndrome (CCHS) is a rare, potentially life-threatening disorder. It affects breathing and other automatic bodily functions as early as infancy or later in life. If you notice that you or your baby has symptoms of CCHS, seek medical attention as soon as possible.
4 Αυγ 2017 · Congenital central hypoventilation syndrome (CCHS), known colloquially as Ondine's curse, is a rare disorder characterized by impaired autonomic control of breathing during sleep from the loss of vagal input and diminished sensitivity of CO 2 receptors in the medulla.
28 Φεβ 2018 · Introduction: Congenital central hypoventilation syndrome (CCHS) is a rare disorder defined by a failure in autonomic control of breathing secondary to mutations of the PHOX2B gene.
What is congenital central hypoventilation syndrome? Congenital central hypoventilation syndrome (CCHS), also known as “Ondine’s curse,” is a rare neurological disorder characterized by inadequate breathing during sleep and in more severely affected individuals, during waking periods as well.
