Literature DB >> 8205323

The acrocallosal syndrome: expansion of the phenotypic spectrum.

I W Lurie1, I V Naumchik, E A Wulfsberg.   

Abstract

A family demonstrating the acrocallosal syndrome in a female proband whose sister had anencephaly is described. Two similar cases were found in the literature (Gelman-Kohan et al., 1991; Cataltepe and Tuncbilek, 1992). Analysis of the multiplex family data suggests that anencephaly may be an extreme manifestation of the spectrum of brain anomalies associated with the acrocallosal syndrome.

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Year:  1994        PMID: 8205323

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  2 in total

1.  Schinzel acrocallosal syndrome.

Authors:  Sheffali Gulati; Shaji Menon; Madhulika Kabra; Veena Kalra
Journal:  Indian J Pediatr       Date:  2003-02       Impact factor: 1.967

2.  The acrocallosal syndrome in a neonate with further widening of phenotypic expression.

Authors:  Ravish Singhal; Sadbhavna Pandit; Ashok Saini; Paramjit Singh; Neeraj Dhawan
Journal:  Iran J Child Neurol       Date:  2014
  2 in total

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