Αποτελέσματα Αναζήτησης
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.
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.
18 Αυγ 2016 · Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder with failure of central control of breathing and of the autonomic nervous system function due to a mutation in the paired-like homeobox 2B (PHOX2B) gene.
Congenital Central Hypoventilation Syndrome (CCHS) is a rare neurocristopathy characterized by severe hypoventilation and autonomic dysregulation, with typical presentation in the neonatal period, and deficient cognitive skills in school-aged patients.
Congenital central hypoventilation syndrome (CCHS) is a genetic condition often appearing at birth in which the brain fails to properly control breathing to maintain healthy levels of oxygen and carbon dioxide.
29 Σεπ 2022 · Congenital central hypoventilation syndrome (CCHS) is a rare life-threatening genetic disorder characterized by inadequate central respiratory responses to hypercarbia (CO 2) and/or hypoxemia (H +) particularly during sleep with or without broad spectrum of autonomic nervous system (ANS) dysregulations.
Congenital central alveolar hypoventilation in the absence of neuromuscular or lung disease is characterized by normal ventilation while the patient is awake but hypoventilation with normal respiratory rates and shallow breathing (di- minished tidal volume) during sleep. The severity of hypo-
