ROHHAD Syndrome

Hari Krishnan
Hari KrishnanDoctor at St. Elizabeth's Medical Center, Tufts University School of Medicine
Rapid-onset Obesity with Hypothalamic Dysfunction, Hypoventilation and Autonomic Dysregulation (ROHHAD) Syndrome 
Hari Krishnan Nair, 
Visiting Medical Student, 
Department of Neurology, 
Boston Children’s Hospital.
A disorder of autonomic nervous system regulation with endocrine abnormalities.
Epidemiology and Etiopathogenesis
Epidemiology 
A rare condition 
Approximately 100 cases reported in the literature and clinically to date 
Predominantly in patients of Caucasian and Arabic descent 
◦One case each of Japanese, Indian and Malaysian origin
Etiology and Pathogenesis 
No specific cause has been found to date 
PHOX2B mutations, which causes a related disorder Congenital Central Hypoventilation Syndrome, are absent in ROHHAD
Clinical Presentation
Clinical Presentation 
Children are apparently healthy until 1.5 years of age 
Subsequently rapid-onset weight gain (often 30 pounds in 6-12 months) 
◦Invariably the first symptom to appear 
Hyperphagia 
Hypersomnolence
Respiratory manifestations (Median age: 6.2 years) 
Alveolar hypoventilation 
◦Very shallow breathing during sleep 
Cardiorespiratory arrest 
Obstructive sleep apnea
Autonomic dysregulation (Median age: 3.6 years) 
Altered pupillary response to light 
Strabismus 
Altered GI motility 
◦Chronic constipation or diarrhea 
Thermal dysregulation 
◦Hyperthermia or hypothermia 
Altered pain perception
Autonomic dysregulation 
Bradycardia 
Altered sweating 
Adipsic Hypernatremia 
Hyperprolactinemia 
Diabetes insipidus
Cardiac abnormalities 
Arrhythmias 
Blood pressure dysregulation 
Right ventricular hypertrophy secondary to cor pulmonale
Anatomic malformations of ANS 
33-39% 
Tumors of neural crest origin 
◦Ganglioneuromas 
◦Ganglioneuroblastomas 
As late as 7-16 years after the onset of obesity
Neurobehavioral disorders 
Behavioral, mood, and developmental disorders 
Seizures – may be related to episodes of hypoxemia due to inadequate ventilator support 
Ataxia
Diagnostic Modalities
Clinical Testing 
Overnight polysomnography 
◦For signs of obstructive sleep apnea and central hypoventilation 
Imaging of chest and abdomen 
◦To screen for evidence of neural crest tumors 
Cardiac evaluation 
Endocrine evaluation 
◦Water balance regulation 
◦Pituitary function
Sequential comprehensive evaluation 
Annual physiologic assessment during spontaneous breathing awake and during sleep 
72-hour Holter recording annually to evaluate for bradycardia 
Echocardiogram annually 
Neurocognitive testing annually
Management
Treatment 
No specific treatment 
Based on the clinical features and their relative severity 
Multidisciplinary care at a tertiary center
Obesity 
Emphasis to avoid further weight gain 
◦In consultation with a nutritionist and endocrinologist 
◦Recommend only modest exertion, with end tidal carbon dioxide and pulse oximetry 
(as patients do not increase their breathing adequately during physical exertion)
Hypothalamic dysfunction 
Hormone replacement 
◦Growth hormone administration, and dopamine agonists to normalize prolactin levels have not been shown to modify the clinical course 
Strict fluid intake regimen
Breathing deficit 
Artificial ventilation 
◦Intially – during sleep only 
◦Later – continuous support 
Most children – Mask ventilation and BiPAP at night 
Some – 24-hour mechanical ventilation with tracheostomy
Autonomic dysregulation 
Permanent pacemakers for bradycardia 
Careful regulation of ambient temperature 
Neural crest tumors – surgical removal 
◦Has not interrupted the unfolding of the ROHHAD phenotype nor induced recovery from the ROHHAD phenotype
ROHHAD FIGHT Inc. 
www.rohhadfight.org
Thank you
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ROHHAD Syndrome

  • 1. Rapid-onset Obesity with Hypothalamic Dysfunction, Hypoventilation and Autonomic Dysregulation (ROHHAD) Syndrome Hari Krishnan Nair, Visiting Medical Student, Department of Neurology, Boston Children’s Hospital.
  • 2. A disorder of autonomic nervous system regulation with endocrine abnormalities.
  • 4. Epidemiology A rare condition Approximately 100 cases reported in the literature and clinically to date Predominantly in patients of Caucasian and Arabic descent ◦One case each of Japanese, Indian and Malaysian origin
  • 5. Etiology and Pathogenesis No specific cause has been found to date PHOX2B mutations, which causes a related disorder Congenital Central Hypoventilation Syndrome, are absent in ROHHAD
  • 7. Clinical Presentation Children are apparently healthy until 1.5 years of age Subsequently rapid-onset weight gain (often 30 pounds in 6-12 months) ◦Invariably the first symptom to appear Hyperphagia Hypersomnolence
  • 8. Respiratory manifestations (Median age: 6.2 years) Alveolar hypoventilation ◦Very shallow breathing during sleep Cardiorespiratory arrest Obstructive sleep apnea
  • 9. Autonomic dysregulation (Median age: 3.6 years) Altered pupillary response to light Strabismus Altered GI motility ◦Chronic constipation or diarrhea Thermal dysregulation ◦Hyperthermia or hypothermia Altered pain perception
  • 10. Autonomic dysregulation Bradycardia Altered sweating Adipsic Hypernatremia Hyperprolactinemia Diabetes insipidus
  • 11. Cardiac abnormalities Arrhythmias Blood pressure dysregulation Right ventricular hypertrophy secondary to cor pulmonale
  • 12. Anatomic malformations of ANS 33-39% Tumors of neural crest origin ◦Ganglioneuromas ◦Ganglioneuroblastomas As late as 7-16 years after the onset of obesity
  • 13. Neurobehavioral disorders Behavioral, mood, and developmental disorders Seizures – may be related to episodes of hypoxemia due to inadequate ventilator support Ataxia
  • 15. Clinical Testing Overnight polysomnography ◦For signs of obstructive sleep apnea and central hypoventilation Imaging of chest and abdomen ◦To screen for evidence of neural crest tumors Cardiac evaluation Endocrine evaluation ◦Water balance regulation ◦Pituitary function
  • 16. Sequential comprehensive evaluation Annual physiologic assessment during spontaneous breathing awake and during sleep 72-hour Holter recording annually to evaluate for bradycardia Echocardiogram annually Neurocognitive testing annually
  • 18. Treatment No specific treatment Based on the clinical features and their relative severity Multidisciplinary care at a tertiary center
  • 19. Obesity Emphasis to avoid further weight gain ◦In consultation with a nutritionist and endocrinologist ◦Recommend only modest exertion, with end tidal carbon dioxide and pulse oximetry (as patients do not increase their breathing adequately during physical exertion)
  • 20. Hypothalamic dysfunction Hormone replacement ◦Growth hormone administration, and dopamine agonists to normalize prolactin levels have not been shown to modify the clinical course Strict fluid intake regimen
  • 21. Breathing deficit Artificial ventilation ◦Intially – during sleep only ◦Later – continuous support Most children – Mask ventilation and BiPAP at night Some – 24-hour mechanical ventilation with tracheostomy
  • 22. Autonomic dysregulation Permanent pacemakers for bradycardia Careful regulation of ambient temperature Neural crest tumors – surgical removal ◦Has not interrupted the unfolding of the ROHHAD phenotype nor induced recovery from the ROHHAD phenotype
  • 23. ROHHAD FIGHT Inc. www.rohhadfight.org