 Sleep Apnea, Central
"Sleep Apnea, Central" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition associated with multiple episodes of sleep apnea which are distinguished from obstructive sleep apnea (SLEEP APNEA, OBSTRUCTIVE) by the complete cessation of efforts to breathe. This disorder is associated with dysfunction of central nervous system centers that regulate respiration.
| Descriptor ID |
D020182
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| MeSH Number(s) |
C08.618.085.852.800 C10.886.425.800.750.800
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| Concept/Terms |
Sleep Apnea, Central- Sleep Apnea, Central
- Apneas, Central Sleep
- Central Sleep Apneas
- Sleep Apneas, Central
- Apnea, Central
- Apneas, Central
- Central Apnea
- Central Apneas
- Apnea, Central Sleep
- Apnea, Sleep, Central
- Sleep Apnea, Lethal Central
- Central Sleep Apnea
- Central Sleep Apnea Syndrome
- Central Sleep Disordered Breathing
- Hypoventilation, Central Alveolar
- Alveolar Hypoventilation, Central
- Alveolar Hypoventilations, Central
- Central Alveolar Hypoventilation
- Hypoventilations, Central Alveolar
- Ondine Syndrome
- Sleep-Disordered Breathing, Central
- Breathing, Central Sleep-Disordered
- Breathings, Central Sleep-Disordered
- Central Sleep-Disordered Breathing
- Central Sleep-Disordered Breathings
- Sleep Disordered Breathing, Central
- Sleep-Disordered Breathings, Central
- Central Alveolar Hypoventilation Syndrome
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Below are MeSH descriptors whose meaning is more general than "Sleep Apnea, Central".
Below are MeSH descriptors whose meaning is more specific than "Sleep Apnea, Central".
This graph shows the total number of publications written about "Sleep Apnea, Central" by people in this website by year, and whether "Sleep Apnea, Central" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 2005 | 2 | 0 | 2 | | 2006 | 3 | 0 | 3 | | 2007 | 1 | 0 | 1 | | 2008 | 0 | 1 | 1 | | 2009 | 1 | 0 | 1 | | 2010 | 0 | 1 | 1 | | 2011 | 1 | 0 | 1 | | 2012 | 3 | 0 | 3 | | 2013 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 1 | 2 |
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Below are the most recent publications written about "Sleep Apnea, Central" by people in Profiles.
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Johnson J, Patwari PP, Wilkerson M, Silvestri JM. An 8-Month-Old Infant With Respiratory Failure After a Fall. Chest. 2021 11; 160(5):e519-e522.
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Zhou A, Rand CM, Hockney SM, Niewijk G, Reineke P, Speare V, Berry-Kravis EM, Zhou L, Jennings LJ, Yu M, Ceccherini I, Bachetti T, Pennock M, Yap KL, Weese-Mayer DE. Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype-phenotype correlation in congenital central hypoventilation syndrome (CCHS). Genet Med. 2021 09; 23(9):1656-1663.
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Patwari PP, Wolfe LF, Sharma GD, Berry-Kravis E. TECPR2 mutation-associated respiratory dysregulation: more than central apnea. J Clin Sleep Med. 2020 06 15; 16(6):977-982.
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Sivan Y, Zhou A, Jennings LJ, Berry-Kravis EM, Yu M, Zhou L, Rand CM, Weese-Mayer DE. Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family members. Am J Med Genet A. 2019 03; 179(3):503-506.
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Charnay AJ, Antisdel-Lomaglio JE, Zelko FA, Rand CM, Le M, Gordon SC, Vitez SF, Tse JW, Brogadir CD, Nelson MN, Berry-Kravis EM, Weese-Mayer DE. Congenital Central Hypoventilation Syndrome: Neurocognition Already Reduced in Preschool-Aged Children. Chest. 2016 Mar; 149(3):809-15.
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Choi M, Thoma M, Tolekidis G, Byrne RW, Diaz AZ. Successful delivery of adjuvant external beam radiotherapy for ependymoma in a patient with Ondine?s curse. Med Dosim. 2015; 40(4):366-71.
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Weese-Mayer DE, Berry-Kravis EM, Ceccherini I, Keens TG, Loghmanee DA, Trang H. [ATS clinical policy statement: congenital central hypoventilation syndrome. Genetic basis, diagnosis and management]. Rev Mal Respir. 2013 Oct; 30(8):706-33.
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Jones KL, Pivnick EK, Hines-Dowell S, Weese-Mayer DE, Berry-Kravis EM, Santiago T, Nnorom C, Pourcyrous M. A triple threat: Down syndrome, congenital central hypoventilation syndrome, and Hirschsprung disease. Pediatrics. 2012 Nov; 130(5):e1382-4.
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Nirupam N, Sharma R, Chhapola V, Kanwal SK, Berry-Kravis EM, Kumar V. Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis? Indian J Pediatr. 2013 Aug; 80(8):688-90.
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Rand CM, Yu M, Jennings LJ, Panesar K, Berry-Kravis EM, Zhou L, Weese-Mayer DE. Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS). Am J Med Genet A. 2012 Sep; 158A(9):2297-301.
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