Literature DB >> 12116264

Genetic counseling for sex chromosome abnormalities.

Mary G Linden1, Bruce G Bender, Arthur Robinson.   

Abstract

Sex chromosome abnormalities (SCAs) are the most frequently occurring chromosomal abnormalities encountered at both prenatal diagnosis and at birth. Approximately 1/400 newborns has an SCA, and incidence at prenatal diagnosis is even greater, 1/250 to 1/300. Physicians and health providers from various specialties are encountering diagnoses of SCAs with increased frequency as more individuals are becoming identified, both prenatally and postnatally. Because these conditions generally have relatively few serious physical implications and because they are extremely variable, genetic counseling is often more complex and challenging than that occurring with an autosomal abnormality. It is imperative that health professionals have the knowledge of content and methodology to provide appropriate counseling to such individuals and their families. During the period from 1964 to 1975, seven international groups (including the Denver group) screened a total of 199,898 consecutive births and identified 307 individuals with SCA. The Denver group has followed more than 40 such individuals from birth to adulthood. In addition, the Denver group has experience in counseling over 1,000 families with a prenatal diagnosis of SCA. Based on these studies and contacts, guidelines for the counseling of individuals and families with SCA are provided. Accurate information must be presented and the variability and imprecise prognosis recognized. Successful counseling strategies include interfamily contact, viewing photographs, and utilizing support groups. Issues of disclosure, follow-up, and anticipatory guidance should be addressed. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2002        PMID: 12116264     DOI: 10.1002/ajmg.10391

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


  19 in total

1.  Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy.

Authors:  Patricia Anne Boyd; Maria Loane; Ester Garne; Babak Khoshnood; Helen Dolk
Journal:  Eur J Hum Genet       Date:  2010-08-25       Impact factor: 4.246

2.  Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.

Authors:  Faustina Lalatta; Donatella Quagliarini; Emanuela Folliero; Ugo Cavallari; Barbara Gentilin; Pierangela Castorina; Francesca Forzano; Serena Forzano; Enrico Grosso; Valeria Viassolo; Valeria Giorgia Naretto; Stefania Gattone; Florinda Ceriani; Francesca Faravelli; Luigi Gargantini
Journal:  Eur J Pediatr       Date:  2010-05-15       Impact factor: 3.183

Review 3.  Triple X syndrome: a review of the literature.

Authors:  Maarten Otter; Constance T R M Schrander-Stumpel; Leopold M G Curfs
Journal:  Eur J Hum Genet       Date:  2009-07-01       Impact factor: 4.246

Review 4.  Screening for fetal chromosomal and subchromosomal disorders.

Authors:  Sarah Harris; Dallas Reed; Neeta L Vora
Journal:  Semin Fetal Neonatal Med       Date:  2017-11-08       Impact factor: 3.926

5.  Sex chromosomes and the brain: a study of neuroanatomy in XYY syndrome.

Authors:  Daniel M Bryant; Fumiko Hoeft; Song Lai; John Lackey; David Roeltgen; Judith Ross; Allan L Reiss
Journal:  Dev Med Child Neurol       Date:  2012-10-12       Impact factor: 5.449

6.  "How should I tell my child?" Disclosing the diagnosis of sex chromosome aneuploidies.

Authors:  Anna Dennis; Susan Howell; Lisa Cordeiro; Nicole Tartaglia
Journal:  J Genet Couns       Date:  2014-09-03       Impact factor: 2.537

7.  A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.

Authors:  Ian Whitmarsh; Arlene M Davis; Debra Skinner; Donald B Bailey
Journal:  Soc Sci Med       Date:  2007-06-11       Impact factor: 4.634

8.  Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child.

Authors:  Kirsten A Riggan; Sharron Close; Megan A Allyse
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-03-17       Impact factor: 3.908

9.  Brain morphology in children with 47, XYY syndrome: a voxel- and surface-based morphometric study.

Authors:  J-F Lepage; D S Hong; M Raman; M Marzelli; D P Roeltgen; S Lai; J Ross; A L Reiss
Journal:  Genes Brain Behav       Date:  2013-12-06       Impact factor: 3.449

10.  Why do parents prefer to know the fetal sex as part of invasive prenatal testing?

Authors:  Angelique J A Kooper; Jacqueline J P M Pieters; Alex J Eggink; Ton B Feuth; Ilse Feenstra; Lia D E Wijnberger; Robbert J P Rijnders; Rik W P Quartero; Peter F Boekkooi; John M G van Vugt; Arie P T Smits
Journal:  ISRN Obstet Gynecol       Date:  2012-12-12
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