A child with microcephaly, facial dysmorphisms, seizures, and congenital car diopathy is presented. On the basis of skull x-rays, electroencephalogram, trans- illumination of the head, and computed tomography (CT) scan, the diagnosis of semilobar holoprosencephaly was made. The heterogeneous etiology of the disorder is discussed in order to evaluate the recurrence risk. The usefulness of CT scan for the classification in the different types of holoprosencephaly is stressed.
Get full access to this article
View all access options for this article.
References
1.
DeMeyer W., Zeman W., Palmer CGFamilial alobar holoprosencephaly (arhinencephaly) with median cleft lip and palate. Report of patient with 46 chromosomes. Neurology1963;13:913.
2.
Byrd SE, Harwood-Nash DC, Fitz CR, et al. Computed tomography evaluation of holoprosencephaly in infants and children. J Comput Assist Tomogr1977;1:456.
3.
Cohen MM, Jr. An update on the holoprosencephalic disorders. J Pediatr1982;101:865.
4.
Volpe J.Neurology of the newborn. Major problems in clinical pediatrics. Philadelphia: WB Saunders, 1981:3.
5.
Cantù JM, Fragoso R., Garcia-Cruz D., et al. Dominant inheritance of holoprosencephaly. Recent advances and new syndromes. In: Summit RL, Bergsma D, eds. Birth defects original articles series. 1978:215.
6.
Roach E., DeMeyer W., Palmer K., et al. Holoprosencephaly: birth data, genetic and demographic analysis of 30 families. Birth Defects1975; 11:294.
7.
Aubry JP, Aubry MC, Briard ML, et al. Mésure prénatal de la distance interorbitaire par echographie. Appoint dans le depistage des formes mineures d'holoprosencéphalie. J Gent Hum1981;29:395.
8.
Elejalde BR, de Elejalde MM, Hamilton PR, et al. Prenatal diagnosis of cyclopia. Am J Med Genet1983;14:15.