Fetal Alcohol Syndrome (FAS) is one of the most common and devastating birth abnormalities among American children. This paper will provide an in-depth look at FAS, using four reliable sources as a basis of this analysis. The sources used are Streissguth, Jacobson & Jacobson, the National Center on Birth Defects and Developmental Disabilities (NCBDDD), and National Organization on Fetal Alcohol Syndrome (NOFAS). The information obtained from these sources will be compared with the textbook Infants and Children Prenatal Through Middle Childhood (Berk, 2001).
FAS is a combination of birth defects that is associated with consuming alcohol during pregnancy. It is the leading cause of mental retardation and birth defects, and is entirely preventable. About 12,000 infants are born every year with FAS, while three times this number have ARND or ARBD (NOFAS).
Those with FAS have a distinctive set of growth deficiencies, facial abnormalities, and central nervous system (CNS) dysfunction (NOFAS). Facial abnormalities include a thin upper lip, a flat midface, and short eyelid openings (Jacobson & Jacobson). Learning and behavioral problems include difficulties with judgment, attention, and memory, while other neurological problems include bad eye-hand coordination and limited motor skills (NOFAS).
Individuals with FAS can have a variety of defining characteristics. Many people with FAS have characteristic facial features, growth deficiencies, and CNS effects (Streissguth). However, notes Streissguth, "others have only partial manifestations, usually the CNS effects without the characteristic facial features or growth deficiency" (p. 5). Individuals with FAS often score well on language tests, but have difficulty with arithmetic and attention. A substantial number of FAS individuals have an IQ in the low average to average range, and are not mentally retarded (Jacobson & Jacobson).
The terms FAS, fetal alcohol effects (FAE), possible fetal alcohol effects (PFAE), and alcohol-related neurodevelopmental disorder (ARND) are not interchangeable. Notes Streissguth, "Children who have only some of the characteristics of FAS (i.e., not enough for a full diagnosis) are often said to have fetal alcohol effects (FAE) or possible fetal alcohol effects (PFAE)" (p. 5). The terms FAE and PFAE have no distinct distinguishing criteria that make them a separate diagnosis, although they can be as destructive as FAS on the patient. The Institute of Medicine introduced the term alcohol-related neurodevelopmental disorder (ARND) in the mid-1980s, a term that centered in on the CNS characteristics of the disease, rather than growth deficiencies and facial characteristics. ARND is often used synonymously with FAS, but it is important to note that ARND can be caused by factors other than (and including) alcohol, so ARND and FAS are not truly synonyms (Streissguth). The term Alcohol-Related Birth Defects (ARBD) refers to "malformations in the skeletal and major organ systems" (NOFAS).
Like individuals in the general population, people with FAS have a wide variety of talents and abilities. Father, they have a wide range of intellectual and functional capabilities that are often related to the location and degree of brain damage during development. Those with FAS have a number of secondary disabilities, including mental illness, drug and alcohol problems, problems with the law, and drop-outs from school are common (Streissguth).
Despite this wide range of ability, individuals with FAS often have a number of shared characteristics. "They are usually trusting (even overly trusting), loving, and naive despite their years. They can also be grumpy, irritable, and rigid. As a result of their prenatal brain damage they may have difficulty, especially as they mature, in evaluating a situation and using their past experiences to come with the problems at hand. They seem to need more protection, supervision, and structure for a longer period of life than usual" (Streissguth, p. 6).
Individuals with FAS benefit enormously from involved, educated, and caring familial and community support. A large number of individuals with FAS need "ongoing help across the life span - anything from a protective environment to a trusted...
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