Respiratory and cardiovascular indicators of autonomic nervous system dysregulation in familial dysautonomia

2011 ◽  
Vol 47 (7) ◽  
pp. 682-691 ◽  
Author(s):  
Michael S. Carroll ◽  
Anna S. Kenny ◽  
Pallavi P. Patwari ◽  
Jan-Marino Ramirez ◽  
Debra E. Weese-Mayer
2021 ◽  
Vol 6 (2) ◽  
pp. 029-032
Author(s):  
Sarebanha Melodie ◽  
Valente Laura ◽  
Kalra Minnea ◽  
Joseph Layon A ◽  
Crimi Ettore

Familial dysautonomia is a rare autosomal recessive neurodegenerative disease affecting cells of the autonomic nervous system. Patients with this disease are insensitive to pain but their autonomic nervous system is still activated with noxious stimuli. This report details a case of a patient with familial dysautonomia who underwent right ankle open reduction and internal fixation for a bimalleolar right ankle fracture. The patients preoperative and intraoperative course were uneventful but shortly after handoff to the intensive care unit, the patient experienced an autonomic crisis. Management of these patients is complex, requiring maintenance of physiologic homeostasis as well as preventing hemodynamic instability caused by noxious stimuli. Any deviations from baseline may cause an autonomic crisis, as happened in our patient. Herein, we detail the perioperative management of a patient with familial dysautonomia in further detail.


2020 ◽  
Vol 40 (05) ◽  
pp. 473-484
Author(s):  
Frances Lefcort

AbstractInvestigations of the cellular and molecular mechanisms that mediate the development of the autonomic nervous system have identified critical genes and signaling pathways that, when disrupted, cause disorders of the autonomic nervous system. This review summarizes our current understanding of how the autonomic nervous system emerges from the organized spatial and temporal patterning of precursor cell migration, proliferation, communication, and differentiation, and discusses potential clinical implications for developmental disorders of the autonomic nervous system, including familial dysautonomia, Hirschsprung disease, Rett syndrome, and congenital central hypoventilation syndrome.


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