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* At this point in time, there are no surgical options available.{{cite web |url=https://www.stlouischildrens.org/conditions-treatments/anencephaly |title=Anencephaly: Causes, Symptoms, Diagnosis and Treatment for Newborns | St. Louis Childrens Hospital |format= |work= |accessdate=}}
* At this point in time, there are no surgical options available.{{cite web |url=https://www.stlouischildrens.org/conditions-treatments/anencephaly |title=Anencephaly: Causes, Symptoms, Diagnosis and Treatment for Newborns | St. Louis Childrens Hospital |format= |work= |accessdate=}}


==Prevention==
===Prevention===
 
* Recent studies have shown that the addition of [[folic acid]] to the [[diet (nutrition)|diet]] of women of child-bearing age may significantly reduce, although not eliminate, the incidence of [[neural tube defects]]. Therefore, it is recommended that all women of child-bearing age consume 0.4&nbsp;mg of [[folic acid]] daily, especially those attempting to conceive or who may possibly conceive, as this can reduce the risk to 0.03%.<ref>{{NINDS|anencephaly}}</ref>
* Recent studies have shown that the addition of [[folic acid]] to the [[diet (nutrition)|diet]] of women of child-bearing age may significantly reduce, although not eliminate, the incidence of [[neural tube defects]]. Therefore, it is recommended that all women of child-bearing age consume 0.4&nbsp;mg of [[folic acid]] daily, especially those attempting to conceive or who may possibly conceive, as this can reduce the risk to 0.03%.<ref>{{NINDS|anencephaly}}</ref>
* It is not advisable to wait until [[pregnancy]] has begun, since by the time a woman knows she is [[pregnant]], the critical time for the formation of a neural tube defect has usually already passed. A physician may prescribe even higher dosages of [[folic acid]] (4&nbsp;mg/day) for women who have had a previous pregnancy with a neural tube defect.<ref name="pmidPMID: 22439027">{{cite journal| author=Cavalli P| title=Prevention of Neural Tube Defects and proper folate periconceptional supplementation. | journal=J Prenat Med | year= 2008 | volume= 2 | issue= 4 | pages= 40-1 | pmid=PMID: 22439027 | doi= | pmc=3279093 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22439027  }} </ref>
* It is not advisable to wait until [[pregnancy]] has begun, since by the time a woman knows she is [[pregnant]], the critical time for the formation of a neural tube defect has usually already passed. A physician may prescribe even higher dosages of [[folic acid]] (4&nbsp;mg/day) for women who have had a previous pregnancy with a neural tube defect.<ref name="pmidPMID: 22439027">{{cite journal| author=Cavalli P| title=Prevention of Neural Tube Defects and proper folate periconceptional supplementation. | journal=J Prenat Med | year= 2008 | volume= 2 | issue= 4 | pages= 40-1 | pmid=PMID: 22439027 | doi= | pmc=3279093 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22439027  }} </ref>

Revision as of 03:31, 23 June 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ayesha Javid, MBBS[2]

For patient information click here

Anencephaly
The side view of the head of an anencephalic fetus.
Source: https://en.wikipedia.org/
ICD-10 Q00.0
ICD-9 740.0
OMIM 206500
DiseasesDB 705
MeSH C10.500.680.196

Overview

Anencephaly is a cephalic disorder in which there is the partial or total absence of the brain. It is an open neural tube defect occurs when the rostral (head) end of the neural tube fails to close resulting in the absence of a major portion of the brain, skull and spinal cord. Children with this disorder are born without a forebrain, the largest part of the brain consisting mainly of the cerebral hemispheres which is responsible for higher cognitive functions and cerebellum which control balance and movement. However, hindbrain is developed. The remaining brain tissue is often exposed - not covered by bone or skin.

Historical Perspective

Classification

Type of Anencephaly Clinical features
Meroanencephaly[3] Meroanencephaly is a rare form of anencephaly. Fetus born have clinical features including misshapen skull bones and a vascular tissue protuberance called cerebrovasculosa.
Holoanencephaly[3] It is the most common type of anencephaly. In this condition, the entire fetus brain fails to develop except for the brain stem. Usually, infant survives for only one day after birth.
Craniorachischisis[4] It is the most severe type of anencephaly. Along with the cranial defect, fetus also has a defect in the vertebral column exposing the underlying neural tissue. Area cerebrovasculosa and area medullovasculosa fill the areas with cranial and spinal defects.

Pathophysiology

  • The craniofacial abnormalities in anencephaly are caused by abnormal induction by the neural crest cells.[7]

Clinical Features

Differentiating Anencephalopathy from other Disorders

At times, anencephaly could be misdiagnosed with other similar diagnosis such as;

Epidemiology and Demographics

Incidence

In the United States, approximately 1,000 to 2,000 babies are born with anencephaly each year. In 2001, the National Center for Health Statistics reported 9.4 cases among 100,000 live births.[10] Anually, more than 300,000 babies are born with neural tube defects throughout the world.[11]

Demographics

In United States, the highest prevalence has been seen among the Hispanic [12]. Female babies, whites and children born to mothers who are at extreme of ages are more likely to be affected by the disorder. Worldwide, Ireland and British Islands has higher prevalence as compared to Asia and Africa which has a lower prevalence rate.[13]

Recurrence rate

Like any other neural tube defect, the recurrence rate of anencephaly is 2-4 percent if one sibling is affected and 10 percent if two siblings are affected.[14][15] This familial tendency is due to genetics, environmental factors, or both.[16]

Risk Factors

Folate deficiency

Genetics

Neural tube defects do not follow direct patterns of heredity, though there is some indirect evidence of inheritance.[19] Recent animal models indicate a possible association with deficiencies of the transcription factor TEAD2.[20]

The motivation behind studying genetic patterns is the following:

  1. NTDs are consistently prevalent among monozygotic twins as compared to dizygotic twins.[21]
  2. There is a high recurrence rate within families. Statistics show the recurrence risk of 1/20 if one previous pregnancy is affected and 1/10 if two pregnancies are affected in a family.[22]
  3. There is higher female preponderence as compared to the males. [23]

Syndromes

Fever/hyperthermia

Amniotic bands

Pregestational diabetes

Maternal Obesity

Toxins

  • Anencephaly and other physical and mental deformities have also been blamed on high exposure to such toxins as lead, chromium, mercury, and nickel. [31]

Natural History, Complications, Prognosis

  • Anencephalic infants are not aggressively resuscitated as there is very little chance of the infant to achieve a full level of consciousness. Instead, clinicians prefer to provide them with adequate hydration, nutrition and comfort.[33] Artificial ventilation, surgery (to fix any co-existing congenital defects), and medications are not considered an option as they have no role in any improvement.[34] Due to this poor prognosis, couple are discussed about the option of the terminating the pregnancy soon after the prenatal diagnosis is established.[35]

Diagnosis

Diagnostic Criteria

Symptoms

Physical Examination

  • Physical examination may be remarkable for:

Laboratory Findings

Alpha-Fetoprotein

Acetylcholinesterase

AChE is an enzyme contained in blood cells, muscle, and nerve tissue. Its levels can be checked from the amniotic fluid via amniocentesis. An elevation of both AFP and AChE values is highly suggestive and accurate for fetal NTD.

Triple screen

Triple screen is a prenatal screening test which includes 3 biomarkers; AFP, hCG and estradiol. It helps to detect certain congenital anomalies, including neural tube defect. The following table shows the triple screening of neural tube defect and how it is differentiated from other anomalies.[45]

Anomaly AFP hCG Estradiol
NTD Increased Normal Normal
Trisomy 21 Decreased Increased Decreased
Trisomy 18 Decreased Decreased Decreased

Imaging Findings

Ultrasound

Ultrasound provides a definitive diagnosis of anencephaly before birth. It can often be diagnosed through a transvaginal ultrasound performed at 12th week postmenstrual.[46]

The ultrasound findings include:

Anencephaly - frog like appearance on prenatal USG. Source: https://radiopaedia.org

.

Management

So far, prevention is the best management of anencephaly.

Medical Therapy

  • There is no known medical therapy available for anencephaly.

Surgery

  • At this point in time, there are no surgical options available."Anencephaly: Causes, Symptoms, Diagnosis and Treatment for Newborns | St. Louis Childrens Hospital".

Prevention

  • Recent studies have shown that the addition of folic acid to the diet of women of child-bearing age may significantly reduce, although not eliminate, the incidence of neural tube defects. Therefore, it is recommended that all women of child-bearing age consume 0.4 mg of folic acid daily, especially those attempting to conceive or who may possibly conceive, as this can reduce the risk to 0.03%.[48]
  • It is not advisable to wait until pregnancy has begun, since by the time a woman knows she is pregnant, the critical time for the formation of a neural tube defect has usually already passed. A physician may prescribe even higher dosages of folic acid (4 mg/day) for women who have had a previous pregnancy with a neural tube defect.[49]

Pregnancy management

References

  1. Milunsky A, Jick H, Jick SS, Bruell CL, MacLaughlin DS, Rothman KJ; et al. (1989). "Multivitamin/folic acid supplementation in early pregnancy reduces the prevalence of neural tube defects". JAMA. 262 (20): 2847–52. doi:10.1001/jama.262.20.2847. PMID 2478730 PMID: 2478730 Check |pmid= value (help).
  2. Bard JS (1999). "The diagnosis is anencephaly and the parents ask about organ donation: now what? A guide for hospital counsel and ethics committees". West New Engl Law Rev. 21 (1): 49–95. PMID 12774804 PMID 12774804 Check |pmid= value (help).
  3. 3.0 3.1 Isada NB, Qureshi F, Jacques SM, Holzgreve W, Tout MJ, Johnson MP; et al. (1993). "Meroanencephaly: pathology and prenatal diagnosis". Fetal Diagn Ther. 8 (6): 423–8. doi:10.1159/000263862. PMID 8286034 PMID 8286034 Check |pmid= value (help).
  4. 4.0 4.1 Greene ND, Copp AJ (2014). "Neural tube defects". Annu Rev Neurosci. 37: 221–42. doi:10.1146/annurev-neuro-062012-170354. PMC 4486472. PMID 25032496 PMID: 25032496 Check |pmid= value (help).
  5. Neuroectoderm becomes a neural plate."Embryology, Neural Tube - StatPearls - NCBI Bookshelf".
  6. Sadler, T. W. (2006). Langman's medical embryology. Philadelphia: Lippincott Williams & Wilkins. ISBN 9780781794855.
  7. Sarnat HB, Flores-Sarnat L (2005). "Embryology of the neural crest: its inductive role in the neurocutaneous syndromes". J Child Neurol. 20 (8): 637–43. doi:10.1177/08830738050200080101. PMID 16225807 PMID 16225807 Check |pmid= value (help).
  8. 8.0 8.1 Gole RA, Meshram PM, Hattangdi SS (2014). "Anencephaly and its associated malformations". J Clin Diagn Res. 8 (9): AC07–9. doi:10.7860/JCDR/2014/10402.4885. PMC 4225866. PMID 25386414 PMID: 25386414 Check |pmid= value (help).
  9. "Anencephaly | Psychology Wiki | Fandom".a
  10. Mathews TJ, Honein MA, Erickson JD (2002). "Spina bifida and anencephaly prevalence--United States, 1991-2001". MMWR Recomm Rep. 51 (RR-13): 9–11. PMID 12353510 PMID: 12353510 Check |pmid= value (help).
  11. "Health Dimensions of Sex and Reproduction — Christopher J. L. Murray, Alan D. Lopez | Harvard University Press".
  12. population."Folic Acid & Neural Tube Defects: Data & Statistics | CDC".
  13. Frey L, Hauser WA (2003). "Epidemiology of neural tube defects". Epilepsia. 44 Suppl 3: 4–13. doi:10.1046/j.1528-1157.44.s3.2.x. PMID 12790881.
  14. Cowchock S, Ainbender E, Prescott G, Crandall B, Lau L, Heller R; et al. (1980). "The recurrence risk for neural tube defects in the United States: a collaborative study". Am J Med Genet. 5 (3): 309–14. doi:10.1002/ajmg.1320050314. PMID 7405962 PMID: 7405962 Check |pmid= value (help).
  15. Toriello HV, Higgins JV (1983). "Occurrence of neural tube defects among first-, second-, and third-degree relatives of probands: results of a United States study". Am J Med Genet. 15 (4): 601–6. doi:10.1002/ajmg.1320150409. PMID 6614048 PMID: 6614048 Check |pmid= value (help).
  16. Copp AJ, Greene ND (2010). "Genetics and development of neural tube defects". J Pathol. 220 (2): 217–30. doi:10.1002/path.2643. PMC 4239538. PMID 19918803 PMID: 19918803 Check |pmid= value (help).
  17. Copp AJ, Stanier P, Greene ND (2013). "Neural tube defects: recent advances, unsolved questions, and controversies". Lancet Neurol. 12 (8): 799–810. doi:10.1016/S1474-4422(13)70110-8. PMC 4023229. PMID 23790957 PMID: 23790957 Check |pmid= value (help).
  18. Wen SW, Walker M (2004). "Risk of fetal exposure to folic acid antagonists". J Obstet Gynaecol Can. 26 (5): 475–80. doi:10.1016/s1701-2163(16)30658-2. PMID 15151734 PMID: 15151734 Check |pmid= value (help).
  19. Shaffer LG, Marazita ML, Bodurtha J, Newlin A, Nance WE (1990). "Evidence for a major gene in familial anencephaly". Am. J. Med. Genet. 36 (1): 97–101. doi:10.1002/ajmg.1320360119. PMID 2333913.
  20. Kaneko KJ, Kohn MJ, Liu C, Depamphilis ML (2007). "Transcription factor TEAD2 is involved in neural tube closure". Genesis. 45 (9): 577–87. doi:10.1002/dvg.20330. PMID 17868131.
  21. Windham GC, Bjerkedal T, Sever LE (1982). "The association of twinning and neural tube defects: studies in Los Angeles, California, and Norway". Acta Genet Med Gemellol (Roma). 31 (3–4): 165–72. doi:10.1017/s0001566000008254. PMID 6763438 PMID: 6763438 Check |pmid= value (help).
  22. Ross ME, Mason CE, Finnell RH (2017). "Genomic approaches to the assessment of human spina bifida risk". Birth Defects Res. 109 (2): 120–128. doi:10.1002/bdra.23592. PMC 5388593. PMID 27883265 PMID: 27883265 Check |pmid= value (help).
  23. 23.0 23.1 Deak KL, Siegel DG, George TM, Gregory S, Ashley-Koch A, Speer MC; et al. (2008). "Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects". Birth Defects Res A Clin Mol Teratol. 82 (10): 662–9. doi:10.1002/bdra.20511. PMC 2981339. PMID 18937341 PMID: 18937341 Check |pmid= value (help).
  24. Phadke S, Agarwal M (2012). "Neural tube defects: A need for population-based prevention program". Indian J Hum Genet. 18 (2): 145–7. doi:10.4103/0971-6866.100747. PMC 3491283. PMID 23162285 PMID: 23162285 Check |pmid= value (help).
  25. Li DK, Janevic T, Odouli R, Liu L (2003). "Hot tub use during pregnancy and the risk of miscarriage". Am J Epidemiol. 158 (10): 931–7. doi:10.1093/aje/kwg243. PMID 14607798 PMID: 14607798 Check |pmid= value (help).
  26. Edwards MJ (2006). "Review: Hyperthermia and fever during pregnancy". Birth Defects Res A Clin Mol Teratol. 76 (7): 507–16. doi:10.1002/bdra.20277. PMID 16933304 PMID: 16933304 Check |pmid= value (help).
  27. Feldkamp ML, Meyer RE, Krikov S, Botto LD (2010). "Acetaminophen use in pregnancy and risk of birth defects: findings from the National Birth Defects Prevention Study". Obstet Gynecol. 115 (1): 109–15. doi:10.1097/AOG.0b013e3181c52616. PMID 20027042 .PMID: 20027042 Check |pmid= value (help).
  28. "StatPearls". 2020. PMID 32310363 Check |pmid= value (help).
  29. Sukanya S, Bay BH, Tay SS, Dheen ST (2012). "Frontiers in research on maternal diabetes-induced neural tube defects: Past, present and future". World J Diabetes. 3 (12): 196–200. doi:10.4239/wjd.v3.i12.196. PMC 3538985. PMID 23301121 PMID: 23301121 Check |pmid= value (help).
  30. Moussa, Hind N; Hosseini Nasab, Susan; Haidar, Ziad A; Blackwell, Sean C; Sibai, Baha M (2016). "Folic acid supplementation: what is new? Fetal, obstetric, long-term benefits and risks". Future Science OA. 2 (2). doi:10.4155/fsoa-2015-0015. ISSN 2056-5623.
  31. Goldsmith, Alexander (1996, quoted by Millen and Holtz, "Dying for Growth")
  32. "Applications of Mass Spectrometry in Life Safety | SpringerLink".
  33. "Anencephaly | Psychology Wiki | Fandom".
  34. "Anencephaly: Causes, Symptoms, Diagnosis and Treatment for Newborns | St. Louis Childrens Hospital".
  35. Machado IN, Martinez SD, Barini R (2012). "Anencephaly: do the pregnancy and maternal characteristics impact the pregnancy outcome?". ISRN Obstet Gynecol. 2012: 127490. doi:10.5402/2012/127490. PMC 3302112. PMID 22462001 PMID: 22462001 Check |pmid= value (help).
  36. "Anencephaly | Radiology Reference Article | Radiopaedia.org".
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  44. Gitlin D, Perricelli A, Gitlin GM (1972). "Synthesis of -fetoprotein by liver, yolk sac, and gastrointestinal tract of the human conceptus". Cancer Res. 32 (5): 979–82. PMID 4111729 PMID 4111729 Check |pmid= value (help).
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  46. Johnson SP, Sebire NJ, Snijders RJ, Tunkel S, Nicolaides KH (1997). "Ultrasound screening for anencephaly at 10-14 weeks of gestation". Ultrasound Obstet Gynecol. 9 (1): 14–6. doi:10.1046/j.1469-0705.1997.09010014.x. PMID 9060123 PMID: 9060123 Check |pmid= value (help).
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  48. Template:NINDS
  49. Cavalli P (2008). "Prevention of Neural Tube Defects and proper folate periconceptional supplementation". J Prenat Med. 2 (4): 40–1. PMC 3279093. PMID 22439027 PMID: 22439027 Check |pmid= value (help).
  50. Jaquier M, Klein A, Boltshauser E (2006). "Spontaneous pregnancy outcome after prenatal diagnosis of anencephaly". BJOG. 113 (8): 951–3. doi:10.1111/j.1471-0528.2006.01014.x. PMID 16827827 PMID: 16827827 Check |pmid= value (help).
  51. Osathanondh R, Donnenfeld AE, Frigoletto FD, Driscoll SG, Ryan KJ (1980). "Induction of labor with anencephalic fetus". Obstet Gynecol. 56 (5): 655–7. PMID 7432739 PMID: 7432739 Check |pmid= value (help).

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