'Benign' Familial Neonatal Convulsions

Author:

Webb Randall1,Bobele Gary1

Affiliation:

1. Department of Neurology, University of Oklahoma Health Sciences Center, Oklahoma City, OK

Abstract

Nine family members over five generations are described in whom convulsions occurred in the first week of life. Routine studies, including cranial computed tomography and electroencephalography, failed to reveal an etiology in the proband, nor was a specific etiology ever found in other affected family members. All affected individuals developed normally. Three had recurrent seizures outside the first year of life. This condition is of particular importance to those who care for infants with seizures. An appropriate family history should obviate the need for unnecessary diagnostic tests as well as prolonged anticonvulsant therapy, but counseling regarding the increased risk of subsequent seizures should be provided to affected individuals. ( J Child Neurol 1990;5:295-298).

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Reference15 articles.

1. Volpe JJ: Neurology of the Newborn. Philadelphia, WB Saunders, 1981, p 115.

2. Aicardi J.: Epilepsy in Children. New York, Raven Press, 1986, p 197.

3. Familial neonatal and infantile seizures: An autosomal-dominant disorder

4. Brann AW: Factors during neonatal life that influence brain disorders. In Freeman JM (ed). Prenatal and Perinatal Factors Associated with Brain Disorders. Bethesda, US Department of Public Health, 1985, p 284.

5. Holmes GL: Diagnosis and Management of Seizures in Children. Philadelphia , WB Saunders, p 255.

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