Dictionary:
an·en·ceph·a·ly (ăn'ən-sĕf'ə-lē)
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Neurological Disorder:
Anencephaly |
Definition
Anencephaly is a lethal birth defect characterized by the absence of all or part of the skull and scalp and malformation of the brain.
Description
Anencephaly is one of a group of malformations of the central nervous system collectively called neural tube defects. Anencephaly is readily apparent at birth because of the absence of the skull and scalp and exposure of the underlying brain. The condition is also called acrania (absence of the skull) and acephaly (absence of the head). In its most severe form, the entire skull and scalp are missing. In some cases, termed "meroacrania" or "meroanencephaly," a portion of the skull may be present. In most instances, anencephaly occurs as an isolated birth defect with the other organs and tissues of the body forming correctly. In approximately 10% of cases, other malformations coexist with anencephaly.
Demographics
Anencephaly occurs in all races and ethnic groups. The prevalence rates range from less than one in 10,000 births (European countries) to more than 10 per 10,000 births (Mexico, China).
Causes and symptoms
As an isolated defect, anencephaly appears to be caused by a combination of genetic factors and environmental influences that predispose to faulty formation of the nervous system. The specific genes and environmental insults that contribute to this multifactorial causation are not completely understood. It is known that nutritional insufficiency, specifically folic acid insufficiency, is one predisposing environmental factor, and that mutations of genes involved in folic acid metabolism are genetic risk factors. The recurrence risk after the birth of an infant with anencephaly is 3–5%. The recurrence may be anencephaly or another neural tube defect such as spina bifida.
Anencephaly is readily apparent at birth because of exposure of all or part of the brain. Not only is the brain malformed, but it is also damaged because of the absence of the overlying protective encasement.
Diagnosis
Anencephaly is diagnosed by observation. Prenatal diagnosis may be made by ultrasound examination after 12–14 weeks' gestation. Prenatal diagnosis of anencephaly can also be detected through maternal serum alpha-feto-protein screening. The level of alpha-fetoprotein in the maternal blood is elevated because of the leakage of this fetal protein into the amniotic fluid.
There are no treatments for anencephaly. A pregnant woman or couple expecting an anencephalic baby will need a sensitive and supportive health care team, and perhaps some additional psychological support as they face the inevitable death of their infant, usually before or shortly after birth.
Treatment and management
No treatment is indicated for anencephaly. Affected infants are stillborn or die within the first few days of life. The risk for occurrence or recurrence of anencephaly may be reduced by half or more by the intake of folic acid during the months immediately before and after conception. Natural folic acid, a B vitamin, may be found in many foods (green leafy vegetables, legumes, orange juice, liver). Synthetic folic acid may be obtained in vitamin preparations and in certain fortified breakfast cereals. In the United States, all enriched cereal grain flours have been fortified with folic acid.
Clinical Trials
Research is primarily directed at understanding the underlying factors that affect early neurological development in the fetus.
Prognosis
Anencephaly is uniformly fatal at birth or soon thereafter.
Resources
PERIODICALS
Czeizel, A. E., and I. Dudas. "Prevention of the First Occurrence of Neural Tube Defects by Preconceptional Vitamin Supplementation." New England Journal of Medicine 327 (1992): 1832–1835.
Medical Research Council Vitamin Study Research Group. "Prevention of Neural Tube Defects: Results of the Medical Research Council Vitamin Study." Lancet 338 (1991): 131–137.
Sells, C. J., and J. G. Hall. "Neural Tube Defects." Mental Retardation and Developmental Disabilities Research Reviews 4, no. 4, 1998.
ORGANIZATIONS
March of Dimes Birth Defects Foundation. 1275 Mamaroneck Ave., White Plains, NY 10605. (888) 663-4637. resourcecenter@modimes.org. http://www.modimes.org.
National Birth Defects Prevention Network. Atlanta, GA. (770) 488-3550. http://www.nbdpn.org.
Roger E. Stevenson, MD
Rosalyn Carson-Dewitt, MD
| Veterinary Dictionary: anencephaly |
Congenital absence of the cranial vault, with the cerebral hemispheres completely missing or reduced to small masses.
| Obscure Words: anencephalic |
| Wikipedia: Anencephaly |
| Anencephaly | |
|---|---|
| Classification and external resources | |
| ICD-10 | Q00.0 |
| ICD-9 | 740.0 |
| OMIM | 206500 |
| DiseasesDB | 705 |
| eMedicine | neuro/639 |
| MeSH | C10.500.680.196 |
Anencephaly is a cephalic disorder that results from a neural tube defect that occurs when the cephalic (head) end of the neural tube fails to close, usually between the 23rd and 26th day of pregnancy, resulting in the absence of a major portion of the brain, skull, and scalp[1]. Children with this disorder are born without a forebrain, the largest part of the brain consisting mainly of the cerebral hemispheres (which include the isocortex, which is responsible for higher-level cognition, i.e., thinking). The remaining brain tissue is often exposed—not covered by bone or skin.[2]
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The National Institute of Neurological Disorders and Stroke (NINDS) describes the presentation of this condition as follows:
A baby born with anencephaly is usually blind, deaf, unconscious, and unable to feel pain. Although some individuals with anencephaly may be born with a main brain stem, the lack of a functioning cerebrum permanently rules out the possibility of ever gaining consciousness. Reflex actions such as breathing and responses to sound or touch occur.[2]
Anencephaly can often be diagnosed before birth through an ultrasound examination. The maternal serum alpha-fetoprotein (AFP screening)[3] and detailed fetal ultrasound[4] can be useful for screening for neural tube defects such as spina bifida or anencephaly.
There is no cure or standard treatment for anencephaly and the prognosis for patients is poor. Most anencephalic babies do not survive birth, accounting for 55% of non-aborted cases. If the infant is not stillborn, then he or she will usually die within a few hours or days after birth from cardiorespiratory arrest.
In almost all cases, anencephalic infants are not aggressively resuscitated since there is no chance of the infant ever achieving a conscious existence. Instead, the usual clinical practice is to offer hydration, nutrition and comfort measures and to "let nature take its course". Artificial ventilation, surgery (to fix any co-existing congenital defects), and drug therapy (such as antibiotics) are usually regarded as futile efforts. Clinicians and medical ethicists may view the provision of nutrition and hydration as medically futile.
In the United States, approximately 1 out of 150,000 to 200,000 babies are born with anencephaly each year. Research has suggested that, overall, female babies are more likely to be affected by the disorder.[5]
The cause of anencephaly is disputed. Generally, neural tube defects do not follow direct patterns of heredity, though there is some indirect evidence of inheritance[6], and recent animal models indicating a possible association with deficiencies of the transcription factor TEAD2.[7] Studies show that a woman who has had one child with a neural tube defect such as anencephaly has about a 3% risk of having another child with a neural tube defect.[citation needed]
It is known that women taking certain medication for epilepsy and women with insulin-dependent diabetes have a higher chance of having a child with a neural tube defect.[citation needed] Genetic counseling is usually offered to women at a higher risk of having a child with a neural tube defect to discuss available testing.
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,[2] especially those attempting to conceive or who may possibly conceive, as this can reduce the risk to 0.03%.[citation needed] 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.[original research?]
Anencephaly and other physical and mental deformities have also been blamed on a high exposure to such toxins as lead, chromium, mercury, and nickel.[8]
Until recently, medical literature did not indicate a connection among many genetic disorders, both genetic syndromes and genetic diseases, that are now being found to be related. As a result of new genetic research, some of these are, in fact, highly related in their root cause despite the widely varying set of medical symptoms that are clinically visible in the disorders. Anencephaly is one such disease, part of an emerging class of diseases called ciliopathies. The underlying cause may be a dysfunctional molecular mechanism in the primary cilia structures of the cell, organelles which are present in many cellular types throughout the human body. The cilia defects adversely affect "numerous critical developmental signaling pathways" essential to cellular development and thus offer a plausible hypothesis for the often multi-symptom nature of a large set of syndromes and diseases. Known ciliopathies include primary ciliary dyskinesia, Bardet-Biedl syndrome, polycystic kidney and liver disease, nephronophthisis, Alstrom syndrome, Meckel-Gruber syndrome and some forms of retinal degeneration.[9]
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![]() | Neurological Disorder. Gale Encyclopedia of Neurological Disorders. Copyright © 2005 by The Gale Group, Inc. All rights reserved. Read more | |
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