Literature DB >> 8524711

Atrioventricular septal defect and type A postaxial polydactyly without other major associated anomalies: a specific association.

S E Levin1, R Dansky, S Milner, A Benatar, K Govendrageloo, J du Plessis.   

Abstract

Four children are described, (three black and one white, two boys and two girls) with type A postaxial polydactyly. All four of them, in addition, had either a partial or complete atrioventricular septal defect (AVSD). None of these children had associated major malformations. Minor anomalies were observed (e.g., two patients with hypersegmentation of the sternal segments, one patient with undescended testes, one patient with hypoplastic lumbar vertebra, and one patient with a degree of craniofacial abnormality). Chromosome analysis was carried out for three of the four patients, and was normal in all of them. It is suggested that there is a specific association between type A postaxial polydactyly and the AVSD found in each of these patients. This picture does not conform to, but bears some resemblance to, the Ellis-van Creveld syndrome.

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Year:  1995        PMID: 8524711     DOI: 10.1007/BF00795716

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  13 in total

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Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

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Journal:  Am J Dis Child       Date:  1968-01

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Authors:  D O Sillence
Journal:  Am J Med Genet       Date:  1980

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Authors:  J G Kromberg; T Jenkins
Journal:  S Afr Med J       Date:  1982-10-16

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Authors:  M J Seller
Journal:  Clin Genet       Date:  1981-07       Impact factor: 4.438

9.  Ellis-van Creveld syndrome: report of 15 cases in an inbred kindred.

Authors:  E O da Silva; D Janovitz; S C de Albuquerque
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318

10.  Short rib-polydactyly syndrome: a single or heterogeneous entity? A re-evaluation prompted by four new cases.

Authors:  R Bernstein; J Isdale; M Pinto; J Du Toit Zaaijman; T Jenkins
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

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  5 in total

1.  Atrioventricular canal defect and postaxial polydactyly indicating phenotypic overlap of Ellis-van Creveld and Kaufman-McKusick syndromes.

Authors:  M C Digilio; B Marino; A Giannotti; B Dallapiccola
Journal:  Pediatr Cardiol       Date:  1997 Jan-Feb       Impact factor: 1.655

Review 2.  22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects.

Authors:  Carolina Putotto; Flaminia Pugnaloni; Marta Unolt; Stella Maiolo; Matteo Trezzi; Maria Cristina Digilio; Annapaola Cirillo; Giuseppe Limongelli; Bruno Marino; Giulio Calcagni; Paolo Versacci
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3.  Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome.

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Journal:  Am J Hum Genet       Date:  2020-10-14       Impact factor: 11.025

4.  Fetal Hand Abnormalities in the First-Trimester Scan: A Report of Two Cases.

Authors:  Emmanouil Katsanevakis; Caterina Tzitzikalakis; Natalia Karagioti; Maria Tziomaki; Panagiotis Perdikaris; Anna Papanikolaou; Panagiotis Gkogkos; Nikolaos Tsagkas
Journal:  Cureus       Date:  2022-03-15

Review 5.  Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights.

Authors:  Giulio Calcagni; Flaminia Pugnaloni; Maria Cristina Digilio; Marta Unolt; Carolina Putotto; Marcello Niceta; Anwar Baban; Francesca Piceci Sparascio; Fabrizio Drago; Alessandro De Luca; Marco Tartaglia; Bruno Marino; Paolo Versacci
Journal:  Genes (Basel)       Date:  2021-07-08       Impact factor: 4.096

  5 in total

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