Literature DB >> 24234481

Recommendations for standardized human pedigree nomenclature.

R L Bennett1, K A Steinhaus, S B Uhrich, C K O'Sullivan, R G Resta, D Lochner-Doyle, D S Markel, V Vincent, J Hamanishi.   

Abstract

The construction of an accurate family pedigree is a fundamental component of a clinical genetic evaluation and of human genetic research. Previous surveys of genetic counselors and human genetic publications have demonstrated significant inconsistencies in the usage of common pedigree symbols representing situations such as pregnancy, termination of pregnancy, miscarriage, and adoption, as well as less common scenarios such as pregnancies conceived through assisted reproductive technologies. The Pedigree Standardization Task Force (PSTF) was organized through the Professional Issues Committee of the National Society of Genetic Counselors, to establish recommendations for universal standards in human pedigree nomenclature. Nomenclature was chosen based on current usage, consistency among symbols, computer compatibility, and the adaptability of symbols to reflect the rapid technical advances in human genetics. Preliminary recommendations were presented for review at three national meetings of human genetic professionals and sent to >100 human genetic professionals for review. On the basis of this review process, the recommendations of the PSTF for standardized human pedigree nomenclature are presented here. By incorporating these recommendations into medical genetics professional training programs, board examinations, genetic publications, and pedigree software, the adoption of uniform pedigree nomenclature can begin. Usage of standardized pedigree nomenclature will reduce the chances for incorrect interpretation of patient and family medical and genetic information. It may also improve the quality of patient care provided by genetic professionals and facilitate communication between researchers involved with genetic family studies.

Entities:  

Year:  1995        PMID: 24234481     DOI: 10.1007/BF01408073

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  3 in total

1.  The crane's foot: The rise of the pedigree in human genetics.

Authors:  R G Resta
Journal:  J Genet Couns       Date:  1993-12       Impact factor: 2.537

Review 2.  Inconsistencies in pedigree symbols in human genetics publications: a need for standardization.

Authors:  K A Steinhaus; R L Bennett; R G Resta; S B Uhrich; D L Doyle; D S Markel; V A Vincent
Journal:  Am J Med Genet       Date:  1995-04-10

3.  The need for developing standardized family pedigree nomenclature.

Authors:  R L Bennett; K A Steinhaus; S B Uhrich; C O'Sullivan
Journal:  J Genet Couns       Date:  1993-12       Impact factor: 2.537

  3 in total
  9 in total

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Authors:  Dawna M Gilchrist
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2.  Non-Biological (Fictive Kin and Othermothers): Embracing the Need for a Culturally Appropriate Pedigree Nomenclature in African-American Families.

Authors:  Ida J Spruill; Bernice L Coleman; Yolanda M Powell-Young; Tiffany H Williams; Gayenell Magwood
Journal:  J Natl Black Nurses Assoc       Date:  2014-12

3.  Pathogenicity of new BEST1 variants identified in Italian patients with best vitelliform macular dystrophy assessed by computational structural biology.

Authors:  Vladimir Frecer; Giancarlo Iarossi; Anna Paola Salvetti; Paolo Enrico Maltese; Giulia Delledonne; Marta Oldani; Giovanni Staurenghi; Benedetto Falsini; Angelo Maria Minnella; Lucia Ziccardi; Adriano Magli; Leonardo Colombo; Fabiana D'Esposito; Jan Miertus; Francesco Viola; Marcella Attanasio; Emilia Maggio; Matteo Bertelli
Journal:  J Transl Med       Date:  2019-10-01       Impact factor: 5.531

4.  A novel mutation in RDH5 gene causes retinitis pigmentosa in consanguineous Pakistani family.

Authors:  Neelam Sultan; Irfan Ali; Shazia Anwer Bukhari; Shahid Mahmood Baig; Muhammad Asif; Muhammad Qasim; Muhammad Imran Naseer; Mahmood Rasool
Journal:  Genes Genomics       Date:  2018-02-03       Impact factor: 1.839

5.  Secondary Students' Reasoning on Pedigree Problems.

Authors:  Justin Timm; Katharina Wools; Philipp Schmiemann
Journal:  CBE Life Sci Educ       Date:  2022-03       Impact factor: 3.955

6.  Identification of a balanced complex chromosomal rearrangement involving chromosomes 3, 18 and 21 with recurrent abortion: case report.

Authors:  Yaping Liao; Liqun Wang; Ding Zhang; Changqing Liu
Journal:  Mol Cytogenet       Date:  2014-06-05       Impact factor: 2.009

7.  f-treeGC: a questionnaire-based family tree-creation software for genetic counseling and genome cohort studies.

Authors:  Tomoharu Tokutomi; Akimune Fukushima; Kayono Yamamoto; Yasushi Bansho; Tsuyoshi Hachiya; Atsushi Shimizu
Journal:  BMC Med Genet       Date:  2017-07-14       Impact factor: 2.103

8.  Association of follistatin and cytochrome p450 side-chain cleavage enzyme with polycystic ovarian syndrome.

Authors:  Fouzia Nazir; S Inayatullah; S Jalali
Journal:  Int J Health Sci (Qassim)       Date:  2022 Sep-Oct

Review 9.  Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors.

Authors:  Heather B Radtke; Courtney D Sebold; Caroline Allison; Joy Larsen Haidle; Gretchen Schneider
Journal:  J Genet Couns       Date:  2007-07-17       Impact factor: 2.537

  9 in total

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