Ondine's curse
Information about Ondine's curse
| Ondine, by John William Waterhouse (1872) | |
| ICD-10 | G47.3 |
| ICD-9 | 348.8 |
| OMIM | 209880 |
| DiseasesDB | 32976 |
| MedlinePlus | 000078 |
| eMedicine | ped/1645 |
| MeSH | D020182 |
Ondine's Curse, also called congenital central hypoventilation syndrome (CCHS) or primary alveolar hypoventilation, is a respiratory disorder that is fatal if untreated. Persons afflicted with Ondine's curse classically suffer from respiratory arrest during sleep.
This very rare and serious form of central sleep apnea involves an inborn failure of autonomic control of breathing. About 1 in 200,000 live born children have the condition. In 2006, there were only about 200 known cases worldwide. In all cases, episodes of apnea occur in sleep, but in a few patients, at the most severe end of the spectrum, apnea also occurs while awake.
Symptoms
Ondine's curse is associated with respiratory arrests during sleep and, with incomplete penetrance, neuroblastoma (tumors of the sympathetic ganglia), Hirschprung disease (partial agenesis of the enteric nervous system), dysphagia (difficulty swallowing), anomalies of the pupilla, etc.Causes
Ondine's curse is exhibited typically as a congenital disorder, but in rare circumstances, can also result from severe brain or spinal trauma (such as after an automobile accident, stroke, or an error made during neurosurgery).Medical investigation of patients with this syndrome has led to a deeper understanding of how the body and brain regulate breathing on a molecular level. PHOX2B can be associated with this condition.[1][2][3][4] This homeobox gene is important for the normal development of the autonomic nervous system.
The disease used to be classified as a "neurocristopathy",[5][6] or disease of the neural crest because part of the autonomic nervous system (such as sympathetic ganglia) derives from the neural crest. However, this denomination should be dropped because essential neurons of the autonomic nervous system, including those that underlie the defining symptom of the disease (respiratory arrests), are derived from the neural tube (the medulla), not from the neural crest.
Diagnosis
Children with Congenital Central Hypoventilaion Syndrome develop life-threatening episodes of apnea with cyanosis, usually in the first months of life. Medical evaluation excludes lesions of the brain, heart, and lungs but demonstrate impaired responses to build-up of carbon dioxide (hypercapnia) and decreases of oxygen in the circulation (hypoxia), the two strongest stimuli to increase breathing rate.Polysomnography shows that hypoventilation is most marked during slow-wave sleep. In the most severe cases, hypoventilation is present during other nonrapid eye movement sleep stages and even wakefulness. A subset of CCHS patients are at very high risk for developing malignant neural crest derived tumors, such as neuroblastoma.
The sequence of PHOX2B reveals mutations in 91% of the cases.[7]
As in many disorders that are very rare, an infant with this unusual form of sleep apnea suffers from the probability that their physician has most likely never seen another case and will not recognize the diagnosis. In some locations, such as France, optimal management of patients, once identified, has been aided by the creation of a national registry and the formation of a network of centers.
Treatment and prognosis
Patients generally require tracheotomies and lifetime mechanical ventilation on a respirator in order to survive. However, it is now been shown that Biphasic Cuirass Ventilation can effectively be used without the need of a tracheotomy.Most people with congenital Ondine's curse do not survive infancy, unless they receive ventilatory assistance during sleep. An alternative to a mechanical ventilator is Phrenic Nerve Pacing/diaphragm pacing.[8]
Although rare, cases of long-term untreated CCHS have been reported.[9]
History and etymology
It was first described in 1962 by Severinghaus and Mitchell in three patients following surgery to the upper cervical spinal cord and brainstem.[10]Its name is a reference to the myth of Ondine,[11] a water nymph who had an unfaithful mortal lover. He swore to her that his "every waking breath would be a testimony of [his] love", and upon witnessing his adultery, she cursed that if he should fall asleep, he would forget to breathe. Eventually, he fell asleep from sheer exhaustion, and his breathing stopped.
Cultural references
- Ondine's curse was mentioned in the 1987 film Black Widow starring Debra Winger, Theresa Russell, Terry O'Quinn and D. W. Moffett. Ondine's Curse was given as a reason for the death of a mafia connected man who suddenly died in his sleep for no reason.
- Ondine's curse was also mentioned in the book It's Kind of A Funny Story (Ned Vizzini). The main character describes the phenomenon after having read it in DSM (the Diagnostic and Statistical Manual), a psychiatric textbook.
References
1. ^ Gaultier C, Amiel J, Dauger S, et al (2004). "Genetics and early disturbances of breathing control". Pediatr. Res. 55 (5): 729-33. DOI:10.1203/01.PDR.0000115677.78759.C5. PMID 14739359.
2. ^ Gaultier C, Trang H, Dauger S, Gallego J (2005). "Pediatric disorders with autonomic dysfunction: what role for PHOX2B?". Pediatr. Res. 58 (1): 1-6. DOI:10.1203/01.PDR.0000166755.29277.C4. PMID 15901893.
3. ^ Todd ES, Weinberg SM, Berry-Kravis EM, et al (2006). "Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology". Pediatr. Res. 59 (1): 39-45. DOI:10.1203/01.pdr.0000191814.73340.1d. PMID 16327002.
4. ^ "Gene secret of 'mythical curse'" at BBC News, 5 May 2003 (The article misspells PHOX2B as "Thox2b".)
5. ^ Kincaid PK, Dietrich RB, Pais MJ (1994). "Pediatric case of the day. Neurocristopathy (Ondine-Hirschsprung syndrome)". Radiographics : a review publication of the Radiological Society of North America, Inc 14 (5): 1139-43. PMID 7991820.
6. ^ Poceta JS, Strandjord TP, Badura RJ, Milstein JM (1987). "Ondine curse and neurocristopathy". Pediatr. Neurol. 3 (6): 370-2. PMID 3508086.
7. ^ Trang H, Dehan M, Beaufils F, Zaccaria I, Amiel J, Gaultier C (2005). "The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype". Chest 127 (1): 72-9. DOI:10.1378/chest.127.1.72. PMID 15653965.
8. ^ Takeda S, Fujii Y, Kawahara H, Nakahara K, Matsuda H (1996). "Central alveolar hypoventilation syndrome (Ondine's curse) with gastroesophageal reflux". Chest 110 (3): 850-2. PMID 8797441.
9. ^ Windisch W, Hennings E, Storre J, Matthys H, Sorichter S. "Long-term survival of a patient with congenital central hypoventilation syndrome despite the lack of continuous ventilatory support.". Respiration 71 (2): 195-8. PMID 15031579.
10. ^ Severinghaus JW, Mitchell RA. Ondine's curse - failure of respiratory center automaticity while awake. Clin Res 1962;10:122.
11. ^ Nannapaneni R, Behari S, Todd NV, Mendelow AD (2005). "Retracing "Ondine's curse"". Neurosurgery 57 (2): 354–63; discussion 354–63. PMID 16094167.
2. ^ Gaultier C, Trang H, Dauger S, Gallego J (2005). "Pediatric disorders with autonomic dysfunction: what role for PHOX2B?". Pediatr. Res. 58 (1): 1-6. DOI:10.1203/01.PDR.0000166755.29277.C4. PMID 15901893.
3. ^ Todd ES, Weinberg SM, Berry-Kravis EM, et al (2006). "Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology". Pediatr. Res. 59 (1): 39-45. DOI:10.1203/01.pdr.0000191814.73340.1d. PMID 16327002.
4. ^ "Gene secret of 'mythical curse'" at BBC News, 5 May 2003 (The article misspells PHOX2B as "Thox2b".)
5. ^ Kincaid PK, Dietrich RB, Pais MJ (1994). "Pediatric case of the day. Neurocristopathy (Ondine-Hirschsprung syndrome)". Radiographics : a review publication of the Radiological Society of North America, Inc 14 (5): 1139-43. PMID 7991820.
6. ^ Poceta JS, Strandjord TP, Badura RJ, Milstein JM (1987). "Ondine curse and neurocristopathy". Pediatr. Neurol. 3 (6): 370-2. PMID 3508086.
7. ^ Trang H, Dehan M, Beaufils F, Zaccaria I, Amiel J, Gaultier C (2005). "The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype". Chest 127 (1): 72-9. DOI:10.1378/chest.127.1.72. PMID 15653965.
8. ^ Takeda S, Fujii Y, Kawahara H, Nakahara K, Matsuda H (1996). "Central alveolar hypoventilation syndrome (Ondine's curse) with gastroesophageal reflux". Chest 110 (3): 850-2. PMID 8797441.
9. ^ Windisch W, Hennings E, Storre J, Matthys H, Sorichter S. "Long-term survival of a patient with congenital central hypoventilation syndrome despite the lack of continuous ventilatory support.". Respiration 71 (2): 195-8. PMID 15031579.
10. ^ Severinghaus JW, Mitchell RA. Ondine's curse - failure of respiratory center automaticity while awake. Clin Res 1962;10:122.
11. ^ Nannapaneni R, Behari S, Todd NV, Mendelow AD (2005). "Retracing "Ondine's curse"". Neurosurgery 57 (2): 354–63; discussion 354–63. PMID 16094167.
John William Waterhouse
John William Waterhouse
1849-04-06
Rome, Italy
1917-02-10
London, England
British
Painter
Royal Academy
Pre-Raphaelite
Hylas and the Nymphs
The Lady of Shalott
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John William Waterhouse
1849-04-06
Rome, Italy
1917-02-10
London, England
British
Painter
Royal Academy
Pre-Raphaelite
Hylas and the Nymphs
The Lady of Shalott
..... Click the link for more information.
For other uses of "ICD", see ICD (disambiguation).
The International Statistical Classification of Diseases and Related Health Problems (most commonly known by the abbreviation ICD
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List of ICD-10 codes. The version for 2007 is available online at [1]
Chapter Blocks Title
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III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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Chapter Blocks Title
I Certain infectious and parasitic diseases
II Neoplasms
III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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The International Statistical Classification of Diseases and Related Health Problems (most commonly known by the abbreviation ICD
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The following is a list of codes for International Statistical Classification of Diseases and Related Health Problems. These codes are in the public domain.
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Respiratory arrest
Classifications and external resources
ICD-10 R 09.2
ICD-9 799.1
Respiratory arrest is the cessation of the normal tidal flow of the lungs due to paralysis of the diaphragm, collapse of the lung or any number of respiratory
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Classifications and external resources
ICD-10 R 09.2
ICD-9 799.1
Respiratory arrest is the cessation of the normal tidal flow of the lungs due to paralysis of the diaphragm, collapse of the lung or any number of respiratory
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MeSH D012891
Sleep apnea, sleep apnoea or sleep apnœa is a sleep disorder characterized by pauses in breathing during sleep. These episodes, called apneas (literally, "without breath"), each last long enough so one or more breaths are missed, and
..... Click the link for more information.
Sleep apnea, sleep apnoea or sleep apnœa is a sleep disorder characterized by pauses in breathing during sleep. These episodes, called apneas (literally, "without breath"), each last long enough so one or more breaths are missed, and
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autonomic nervous system (ANS) (or visceral nervous system) is the part of the peripheral nervous system that acts as a control system, maintaining homeostasis in the body. These maintenance activities are primarily performed without conscious control or sensation.
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Apnea
Classifications and external resources
ICD-10
ICD-9 786.03
Apnea, apnoea, or apnœa (Greek απνοια, from α-, privative, πνεειν, to breathe) is a technical
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Classifications and external resources
ICD-10
ICD-9 786.03
Apnea, apnoea, or apnœa (Greek απνοια, from α-, privative, πνεειν, to breathe) is a technical
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Penetrance is a term used in genetics describing the proportion of individuals carrying a particular variation of a gene (the genotype) that also express a particular trait (the phenotype).
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Neuroblastoma, NOS
Classification & external resources
ICD-10 C 74.9
ICD-9 194.0
ICD-O: M 9500/3
OMIM 256700
DiseasesDB 8935
MedlinePlus 001408
eMedicine med/2836 ped/1570
MeSH D009447 Neuroblastoma
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Classification & external resources
ICD-10 C 74.9
ICD-9 194.0
ICD-O: M 9500/3
OMIM 256700
DiseasesDB 8935
MedlinePlus 001408
eMedicine med/2836 ped/1570
MeSH D009447 Neuroblastoma
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Sympathetic ganglia are the ganglia of the sympathetic nervous system. They deliver information to the body about stress and impending danger, and are responsible for the familiar fight-or-flight response.
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MeSH D006627 Hirschsprung's disease, or congenital aganglionic megacolon, involves an enlargement of the colon, caused by bowel obstruction resulting from an aganglionic section of bowel (the normal enteric nerves are absent) that starts at the anus and progresses
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enteric nervous system (ENS) is the part of the nervous system that directly controls the gastrointestinal system. It is capable of autonomous functions such as the coordination of reflexes, although it receives considerable innervation from the autonomic nervous system and
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Dysphagia
Classifications and external resources
ICD-10 R 13.
ICD-9 787.2
DiseasesDB 17942
MedlinePlus 003115
eMedicine pmr/194
Dysphagia (
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Classifications and external resources
ICD-10 R 13.
ICD-9 787.2
DiseasesDB 17942
MedlinePlus 003115
eMedicine pmr/194
Dysphagia (
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Pupilla is a genus of land gastropods from family Pupillidae.
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Species
- Pupilla alpicola (Charpentier, 1837)
- Pupilla ficulnea (Tate, 1894) - LR/nt [1]
- Pupilla muscorum (Linnaeus, 1758)
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A congenital disorder is any medical condition that is present at birth. However, a congenital disorder can be recognized before birth (prenatally), at birth, years later, or never. The term congenital does not imply or exclude a genetic cause.
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car accident or car crash is an incident in which an automobile collides with anything that causes damage to the automobile, including other automobiles, telephone poles, buildings or trees, or in which the driver loses control of the vehicle and damages it in some other
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Stroke
Classification & external resources
ICD-10 I 61. -I 64.
ICD-9 435 - 436
OMIM 601367
DiseasesDB 2247
MedlinePlus 000726pi
eMedicine neuro/9 emerg/558 emerg/557 pmr/187
MeSH D020521
Stroke (or
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Classification & external resources
ICD-10 I 61. -I 64.
ICD-9 435 - 436
OMIM 601367
DiseasesDB 2247
MedlinePlus 000726pi
eMedicine neuro/9 emerg/558 emerg/557 pmr/187
MeSH D020521
Stroke (or
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Neurosurgery is the surgical discipline focused on treating those central, peripheral nervous system and spinal column diseases amenable to mechanical intervention.
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Definition and scope
According to the U.S...... Click the link for more information.
PHOX2B is a human gene located on chromosome 4.
It codes for a homeodomain transcription factor. It is expressed exclusively in the nervous system, in most neurons that control the viscera (cardiovascular, digestive and respiratory systems).
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It codes for a homeodomain transcription factor. It is expressed exclusively in the nervous system, in most neurons that control the viscera (cardiovascular, digestive and respiratory systems).
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A homeobox is a DNA sequence found within genes that are involved in the regulation of development (morphogenesis) of animals, fungi and plants. Genes that have a homeobox are called homeobox genes and form the homeobox gene family.
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autonomic nervous system (ANS) (or visceral nervous system) is the part of the peripheral nervous system that acts as a control system, maintaining homeostasis in the body. These maintenance activities are primarily performed without conscious control or sensation.
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The neural crest, a transient component of the ectoderm, is located in between the neural tube and the epidermis (or the free margins of the neural folds) of an embryo during neural tube formation.
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autonomic nervous system (ANS) (or visceral nervous system) is the part of the peripheral nervous system that acts as a control system, maintaining homeostasis in the body. These maintenance activities are primarily performed without conscious control or sensation.
..... Click the link for more information.
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neural tube is the embryo's precursor to the central nervous system, which comprises the brain and spinal cord. The neural groove gradually deepens as the neural folds become elevated, and ultimately the folds meet and coalesce in the middle line and convert the groove into a
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