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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.
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.
What are the symptoms of congenital central hypoventilation syndrome? Various signs and symptoms of CCHS tend to appear soon after birth, ranging from brief pauses in breathing (apnoea) or breath-holding spells, to complete failure to breathe after birth.
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.
2 Ιουλ 2024 · Congenital central hypoventilation syndrome (CCHS), also known as Ondine’s curse, is a rare neurological condition characterized by alveolar hypoventilation and autonomic nervous system dysregulation. CHHS is a life-threatening condition that causes an oxygen shortage and an accumulation of carbon dioxide in the blood.
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.
Conditions as- of age were examined by behavioral criteria to determine sociated with congenital central hypoventilation syndrome their state as awake oras non-REM or REM sleep.
