Literature DB >> 7762583

Numerical syndromology: a mathematical approach to the nosology of complex phenotypes.

A Verloes1.   

Abstract

Numerical taxonomy is defined by Sneath and Sokal as the grouping of taxonomic units on the basis of their character states by numerical methods of multivariate data analysis, and syndromology as the study of multiple congenital anomaly (MCA) syndromes and of their nosology. We present here an application of those methods to the analysis of overlapping syndromes. The main advantage of numerical taxonomy is that it allows simultaneous objective and unweighted analysis of multiple traits, giving the possibility to test mathematically the clinical hypotheses about the heterogeneity between closely resembling syndromes and uncovering objective patterns of anomalies, to be compared with the subjective pattern recognition process which characterizes most of the diagnostic approach in syndromology. In this paper, we explored 5 syndromes whose most severe expression belongs to the cerebroacrovisceral early lethality (CAVE) phenotype: hydrolethalus, severe Smith-Lemli-Opitz, orofaciodigital type VI (Varadi-Papp), holoprosencephaly-polydactyly, and Pallister-Hall syndromes. Fifty-five published cases, including many overlapping cases, were submitted to principal factor analysis followed by hierarchical clustering and graphical scaling. Results show that the 5 syndromes clearly constitute independent phenotypic entities, that some of the original diagnoses have to be reconsidered, and that many of the overlapping cases may be unambiguously set in one category. Hypothalamic hamartoblastoma appears to be a nonspecific dysplasia occurring in any of the 5 disorders.

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Year:  1995        PMID: 7762583     DOI: 10.1002/ajmg.1320550410

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  Identification of clinically relevant phenotypes in patients with Ebstein anomaly.

Authors:  Rodrigo Cabrera; Marta Catalina Miranda-Fernández; Victor Manuel Huertas-Quiñones; Marisol Carreño; Ivonne Pineda; Carlos M Restrepo; Claudia Tamar Silva; Rossi Quero; Juan David Cano; Diana Carolina Manrique; Camila Camacho; Sebastián Tabares; Alberto García; Néstor Sandoval; Karen Julieth Moreno Medina; Rodolfo José Dennis Verano
Journal:  Clin Cardiol       Date:  2018-03-22       Impact factor: 2.882

2.  Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.

Authors:  I Visapää; R Salonen; T Varilo; P Paavola; L Peltonen
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

3.  Stringent delineation of Pallister-Hall syndrome in two long surviving patients: importance of radiological anomalies of the hands.

Authors:  A Verloes; A David; L Ngô; A Bottani
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

4.  The many faces of oral-facial-digital syndrome.

Authors:  E Sukarova-Angelovska; N Angelkova; S Palcevska-Kocevska; M Kocova
Journal:  Balkan J Med Genet       Date:  2012-06       Impact factor: 0.519

5.  A graph theory approach to analyze birth defect associations.

Authors:  Dario Elias; Hebe Campaña; Fernando Poletta; Silvina Heisecke; Juan Gili; Julia Ratowiecki; Lucas Gimenez; Mariela Pawluk; Maria Rita Santos; Viviana Cosentino; Rocio Uranga; Monica Rittler; Jorge Lopez Camelo
Journal:  PLoS One       Date:  2020-05-22       Impact factor: 3.240

6.  Syndrome diagnosis: human intuition or machine intelligence?

Authors:  Oivind Braaten; Johannes Friestad
Journal:  Open Med Inform J       Date:  2008-11-19
  6 in total

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