Literature DB >> 25156769

Congenital central hypoventilation syndrome: a neurocristopathy with disordered respiratory control and autonomic regulation.

Casey M Rand1, Michael S Carroll2, Debra E Weese-Mayer3.   

Abstract

Congenital central hypoventilation syndrome (CCHS), a rare neurocristopathy with disordered respiratory control, is characterized by alveolar hypoventilation and diffuse autonomic nervous system (ANS) dysregulation. Mutations in the paired-like homeobox 2B (PHOX2B) are causative, leading to physiologic ANS dysregulation and pathologic abnormalities. Presentation is typically during the newborn period with alveolar hypoventilation during sleep, or in more severely affected individuals, during sleep and wakefulness. Breathing complications occur despite the lungs and airways being normal. Disordered respiratory control demonstrated by absent or severely attenuated ventilatory, behavioral, and arousal responses to both endogenous and exogenous hypoxemia and hypercarbia results in severe physiologic compromise.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Autonomic; CCHS; Hirschsprung; Neuroblastoma; PHOX2B; Respiratory

Mesh:

Substances:

Year:  2014        PMID: 25156769     DOI: 10.1016/j.ccm.2014.06.010

Source DB:  PubMed          Journal:  Clin Chest Med        ISSN: 0272-5231            Impact factor:   2.878


  4 in total

1.  More than meets the eye: infant presenting with hypoxic ischaemic encephalopathy.

Authors:  Kuntal Sen; Rajkumar Agarwal
Journal:  BMJ Case Rep       Date:  2018-04-05

2.  Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndrome.

Authors:  Jacob T Cain; Dae I Kim; Megan Quast; Winnie G Shivega; Ryan J Patrick; Chuanpit Moser; Suzanne Reuter; Myrza Perez; Angela Myers; Jill M Weimer; Kyle J Roux; Megan Landsverk
Journal:  Am J Med Genet A       Date:  2017-03-29       Impact factor: 2.802

3.  Unusual case of central alveolar hypoventilation.

Authors:  Hadil Ak AlOtair; Abdulaziz H Alzeer; Mohammed A Abdou; Shaden O Qasrawi
Journal:  Saudi Med J       Date:  2018-03       Impact factor: 1.484

4.  Structural and functional differences in PHOX2B frameshift mutations underlie isolated or syndromic congenital central hypoventilation syndrome.

Authors:  Simona Di Lascio; Roberta Benfante; Eleonora Di Zanni; Silvia Cardani; Annalisa Adamo; Diego Fornasari; Isabella Ceccherini; Tiziana Bachetti
Journal:  Hum Mutat       Date:  2017-11-21       Impact factor: 4.878

  4 in total

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