Literature DB >> 7351584

The Aicardi syndrome versus congenital infection: diagnostic considerations.

J Willis, N P Rosman.   

Abstract

The Aicardi syndrome consists of agenesis of the corpus callosum, infantile spasms, a characteristic lacunar chorioretinopathy, mental subnormality, and costovertebral anomalies. All patients have been female. Its clinical similarity to several congenital intrauterine infections, particularly toxoplasmosis, is reinforced by the erroneous diagnosis of congenital infection initially made in the two patients reported here. Reasons for this confusion are outlined, and methods for a clinical differentiation between the Aicardi syndrome and the congenital infections are discussed.

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Year:  1980        PMID: 7351584     DOI: 10.1016/s0022-3476(80)80808-0

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  3 in total

1.  Dysgenesis of the corpus callosum.

Authors:  B E Kendall
Journal:  Neuroradiology       Date:  1983       Impact factor: 2.804

2.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Refractory seizures with global developmental delay: A rare cause.

Authors:  P N Vinoth; Betty Chacko; J Julius Xavier Scott
Journal:  Indian J Hum Genet       Date:  2011-09
  3 in total

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