Literature DB >> 12661814

Genetic counseling in acrocallosal syndrome.

Sunita Bijarnia1, Ashok Baijal, I C Verma.   

Abstract

This article reports two families with children having acrocallosal syndrome, an autosomal recessive disorder characterized by agenesis of corpus callosum, facial dysmorphism and polydactyly along with psychomotor retardation. Both families sought genetic counseling in subsequent pregnancies. Although the gene for the disorder is not yet identified, prenatal diagnosis was attempted by ultrasound studies. In both families, an affected fetus was diagnosed in the presence of postaxial polydactyly of hands and absence of corpus callosum. It is emphasized that pediatricians should make precise diagnosis in cases of dysmorphism and mental retardation, as this enable prenatal diagnosis in future pregnancies.

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Year:  2003        PMID: 12661814     DOI: 10.1007/BF02723748

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  8 in total

1.  Sibs with anencephaly, anophthalmia, clefts, omphalocele, and polydactyly: hydrolethalus or acrocallosal syndrome?

Authors:  B Christensen; H G Blaas; C V Isaksen; B Roald; K H Orstavik
Journal:  Am J Med Genet       Date:  2000-03-20

2.  The acrocallosal syndrome in sisters.

Authors:  A Schinzel; U Kaufmann
Journal:  Clin Genet       Date:  1986-11       Impact factor: 4.438

3.  Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome.

Authors:  W Courtens; E Vamos; C Christophe; A Schinzel
Journal:  Am J Med Genet       Date:  1997-03-03

4.  Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.

Authors:  R A Pfeiffer; G Legat; U Trautmann
Journal:  Ann Genet       Date:  1992

5.  Spectrum of the acrocallosal syndrome.

Authors:  Rainer Koenig; Alexia Bach; Ulrike Woelki; Karl-Heinz Grzeschik; Sigrun Fuchs
Journal:  Am J Med Genet       Date:  2002-02-15

6.  Further delineation of the acrocallosal syndrome.

Authors:  Z Gelman-Kohan; J Antonelli; H Ankori-Cohen; H Adar; J Chemke
Journal:  Eur J Pediatr       Date:  1991-09       Impact factor: 3.183

7.  A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity.

Authors:  S Cataltepe; E Tuncbilek
Journal:  Eur J Pediatr       Date:  1992-04       Impact factor: 3.183

8.  The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritance.

Authors:  A Schinzel
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

  8 in total
  3 in total

1.  Acrocallosal syndrome in a young hypertensive male.

Authors:  Vishal V Ramteke; Pramod A Darole; Zohaib Farooqui Shaikh; Namita J Padwal; Brijesh Agrawal; Makardhwaj S Shrivastava; Sandhya Kamath
Journal:  BMJ Case Rep       Date:  2011-05-03

2.  Acro-callous syndrome: A case report.

Authors:  A Lamrissi; F E Madri; M Charkaoui; M Mourabbih; M Jalal; S Bouhya
Journal:  Int J Surg Case Rep       Date:  2022-05-20

3.  Orodental manifestations in cases with partial agenesis of corpus callosum-rare phenomena.

Authors:  Annette M Bhambal; Ajay Bhambal; Preeti Nair; Sheela S Bhambal
Journal:  J Oral Biol Craniofac Res       Date:  2015-06-06
  3 in total

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