Behr syndrome

Fetal alcohol spectrum disorders (FASD) are caused by the effects of maternal alcohol consumption during pregnancy. Fetal alcohol syndrome (FAS) is the most clinically recognizable form of FASD and is characterized by a pattern of minor facial anomalies, prenatal and postnatal growth retardation, and functional or structural central nervous system (CNS) abnormalities. The consequences are lifelong, and the behavioral and learning difficulties are often greater than the degree of neurocognitive impairment. Alcohol-related neurodevelopmental disorder also is a clinically recognizable diagnosis in the continuum of FASD and describes the clinical outcome when the facial features typical of FAS are absent.

Epidemiology

FASD may affect up to 1 percent of the U.S. population. (1,2) Birth defects related to these disorders can be prevented by avoiding alcohol ingestion during pregnancy. Although FASD is more strongly associated with higher levels of alcohol consumption compared with lower levels, animal studies have suggested that even a single episode of consuming the equivalent of two alcoholic drinks during pregnancy may lead to loss of fetal brain cells (one drink = 12 oz of beer, 5 oz of wine, or 1.5 oz of "hard" liquor). (3) Despite widespread knowledge of alcohol's deleterious effects, a study (4) of women between 18 and 44 years of age showed that 10 percent used alcohol during pregnancy and that 2 percent engaged in "binge drinking" (i.e., five or more drinks on one occasion). Maternal factors that increase the risk of FASD include being older than 30 years, a history of binge drinking, and low socioeconomic status. (5)

Clinical Presentation

Clinical findings in a newborn with FAS include a characteristic pattern of facial anomalies, (6,7) with short palpebral fissures, a thin upper lip, and a long, smooth philtrum (Figures 1, 2a through 2d, and 3a through 3c). (4,8) Other findings may include a flat midface, ptosis of the eyelids, epicanthal folds, an upturned nose with a flat nasal bridge, underdeveloped ears ("railroad track" appearance, Figure 4), clinodactyly of the fifth fingers (Figure 5), camptodactyly, "hockey stick" palmar creases (Figure 5), hirsutism, and cardiac defects. Prenatal or postnatal growth retardation typically results in a height or weight below the 10th percentile for age and race. Microcephaly is common, as are structural brain anomalies. CNS impairment may not be apparent in newborns. Cognitive deficits and behavioral anomalies such as attention-deficit/hyperactivity disorder typically become more apparent in school-aged children with FASD and usually persist into adolescence and adulthood, whereas facial findings among the subset with FAS may become less characteristic.

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Diagnosis

Diagnosis of FASD should be considered based on the clinical presentation or suspicion of maternal alcohol exposure. The Centers for Disease Control and Prevention diagnostic criteria for FAS require three specific facial findings (i.e., smooth philtrum, thin vermilion border of the upper lip, and short palpebral fissures), growth deficits, and CNS abnormalities (Table 1 (4) and Figure 3). In the absence of characteristic facial findings, the diagnosis of FASD still should be considered in children with growth problems, CNS abnormalities, and a history of prenatal alcohol exposure.

Because of the associated guilt or stigma, direct questioning or commonly used screening questionnaires such as the four-item CAGE criteria (9) (Cut down, Annoyance, Guilt, Eye-opener) may fail to identify women at risk for delivering a child with FASD. One study (10) showed the T-ACE (Tolerance, Annoyance, Cut down, Eye-opener) assessment to be more effective than other screening tools (Table 2 (10,11)).

Causes of Fetal alcohol spectrum Disorders

FASD is nonhereditary; alcohol causes neuronal damage and cell loss in the fetal brain through direct action as a toxin. No prenatal period has been shown to be safe from the deleterious effects of alcohol. CNS damage may result from alcohol exposure in any trimester, even before the time of a pregnancy test. Women should be advised not to drink from the time of conception to birth.

Although FASD is not inherited, there seems to be a genetic predisposition to problem drinking. For example, in some persons of shared ancestry, such as Native Americans, the similarity in function of shared versions (alleles) of the gene that encodes alcohol dehydrogenase may contribute to an increased risk for alcohol dependence. (12) Additionally, twin studies document similar outcomes in identical twins and different outcomes in nonidentical twins. (6)

Referral and Management

Referral to a multidisciplinary team (i.e., dysmorphologist/clinical geneticist, developmental pediatrician, mental health professional, social worker, and educational specialist) often is necessary for diagnosis because the growth, CNS, and facial features of FASD can overlap other syndromes and disorders. Even in patients who clearly have met diagnostic criteria, referral allows complete assessment for an individualized management plan (Table 3 (4)).

Treatment involves coordination of multiple community services. Social services are needed to ensure a safe home environment and provide parental education. Educational support often is needed most. Early identification and intervention results in significantly improved outcomes. A diagnosis of FAS meets the "presumptive diagnosis" requirements of Part C of the Individuals with Disabilities Education Act, allowing children younger than three years to receive services even if their test results fall in the normal range. After three years of age, eligibility for services often depends on demonstration of a specific functional deficit.

Resources

Additional information about FASD and FAS is available online at the following Web sites:

* Substance Abuse and Mental Health Services Administration

http://fascenter.samhsa.gov

* National Center on Birth Defects and Developmental Disabilities

http://www.cdc.gov/ncbddd/fas

* Fetal Alcohol Syndrome Diagnostic and Prevention Network

http://depts.washington.edu/fasdpn

* National Organization on Fetal Alcohol Syndrome

http://www.nofas.org.

The opinions and assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the U.S. Air Force Medical Service, the U.S. Air Force at large, the National Human Genome Research Institute, or the National Institutes of Health.

The authors thank H. Eugene Hoyme, M.D., and Nasreen Malik, M.D., for assistance with the preparation of the manuscript.

Figures 1, 3a, 4, and 5 provided by Darryl Leja, National Human Genome Research Institute, National Institutes of Health, Bethesda, Md.

Figures 2, 3b, and 3c used with permission from Susan J. Astley, M.D., University of Washington School of Medicine, Seattle.

This article is one in a series coordinated by the National Human Genome Research Institute, National Institutes of Health, Bethesda, Md. Guest editor of the series is Daniel J. Wattendorf, MAJ, MC, USAF.

Author disclosure: Nothing to disclose

REFERENCES

(1.) Sampson PD, Streissguth aP, Bookstein FL, Little RE, Clarren Sk, Dehaene P, et al. incidence of fetal alcohol syndrome and prevalence of alcohol-related neurodevelopmental disorder. Teratology 1997;56:317-26.

(2.) Stratton kR, Howe CJ, Battaglia FC. Fetal alcohol syndrome: diagnosis, epidemiology, prevention, and treatment. Washington, D.C.: national academy Press, 1996.

(3.) Olney JW. Fetal alcohol syndrome at the cellular level. addict Biol 2004;9:137-49.

(4.) National Task Force on Fetal alcohol Syndrome and Fetal alcohol Effect. Fetal alcohol syndrome: guidelines for referral and diagnosis. accessed online May 13, 2005, at: http://www.cdc.gov/ncbddd/fas/documents/ FaS_guidelines_accessible.pdf.

(5.) Sokol RJ, Delaney-Black V, Nordstrom B. Fetal alcohol spectrum disorder. JAMA 2003;290:2996-9.

(6.) Hoyme HE, May Pa, Kalberg Wo, Kodituwakku P, Gossage JP, Trujillo PM, et al. a practical clinical approach to diagnosis of fetal alcohol spectrum disorders: clarification of the 1996 institute of Medicine criteria. Pediatrics 2005;115:39-47.

(7.) Stoler JM, Holmes LB. Recognition of facial features of fetal alcohol syndrome in the newborn. am J Med Genet C Semin Med Genet 2004;127:21-7.

(8.) Astley SJ, Clarren Sk. Diagnosing the full spectrum of fetal alcohol-exposed individuals: introducing the 4-digit diagnostic code. alcohol alcohol 2000;35:400-10.

(9.) Ewing Ja. Detecting alcoholism. The CAGE questionnaire. JAMA 1984;252:1905-7.

(10.) Chang G, Wilkins-Haug L, Berman S, Goetz Ma, Behr H, Hiley a. alcohol use and pregnancy: improving identification. Obstet Gynecol 1998;91:892-8.

(11.) Sokol RJ, Martier SS, Ager JW. The T-ACE questions: practical prenatal detection of risk-drinking. am J Obstet Gynecol 1989;160:863-8.

(12.) Mulligan CJ, Robin RW, osier MV, Sambuughin N, Goldfarb LG, kittles Ra, et al. allelic variation at alcohol metabolism genes (ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian population. Hum Genet 2003;113:325-36.

Genomics Glossary

Camptodactyly: Permanent flexion contracture of a finger or toe.

Clinodactyly: Permanent curving of the fifth finger, usually toward the other fingers; also seen for other fingers or toes.

Epicanthal folds: Skinfolds covering the inner corners of the eyes. Epicanthal folds occur commonly in infants and may persist in persons of certain ancestries.

"Hockey stick" palmar crease: Transverse flexion crease of the palm close to the fingers; widens like the end of a hockey stick and ends between the second and third fingers.

Palpebral fissure length: Distance between the inner and outer corners of one eye.

Philtrum: Vertical groove between the nose and upper lip; a flat or smooth philtrum can present in persons with fetal alcohol spectrum disorders.

Ptosis: Drooping of the upper eyelids.

"Railroad track" ears: The top part (curve) of the outer ear is underdeveloped, folded over, and parallel to the curve beneath it, giving the appearance of a railroad track. Vermilion border: Edge of the lip where it meets the skin of the face.

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