Aicardi's Syndrome: Case Report, Clinical Features, and Electrophysiologic Studies

Richard Weleber, Everett W. Lovrien, John B. Isom

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Aicardi's syndrome consists of abnormalities of the ocular fundus, myoclonic seizures, mental retardation, and congenital malformations of the brain and vertebral column in females. The pathognomonic chorioretinal lesions were noted on ophthalmologic examination of a 22-month-old girl, observed for 19 months with severe myoclonic seizures and profound mental retardation. Computerized tomography confirmed major malformation of the brain. Roentgenograms showed anterior fusion of two thoracic vertebrae. Electroretinography was normal, but visual evoked responses were abnormal. Only 72 children are known to have this syndrome; no affected siblings have been reported. The absolute sex limitation—all cases have been female—suggests that the disorder is produced by a mutation on one of the X chromosomes, and is nonviable in male conceptuses. These genetic considerations dramatically influence counseling of parents regarding likelihood of occurrence of the syndrome in subsequent offspring.

Original languageEnglish (US)
Pages (from-to)285-290
Number of pages6
JournalArchives of Ophthalmology
Volume96
Issue number2
DOIs
StatePublished - 1978

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Aicardi Syndrome
Intellectual Disability
Seizures
Thoracic Vertebrae
Electroretinography
Visual Evoked Potentials
Brain
X Chromosome
Counseling
Siblings
Spine
Parents
Tomography
Mutation

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Aicardi's Syndrome : Case Report, Clinical Features, and Electrophysiologic Studies. / Weleber, Richard; Lovrien, Everett W.; Isom, John B.

In: Archives of Ophthalmology, Vol. 96, No. 2, 1978, p. 285-290.

Research output: Contribution to journalArticle

Weleber, Richard ; Lovrien, Everett W. ; Isom, John B. / Aicardi's Syndrome : Case Report, Clinical Features, and Electrophysiologic Studies. In: Archives of Ophthalmology. 1978 ; Vol. 96, No. 2. pp. 285-290.
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