Literature DB >> 32468478

Genetic Counseling for Adult-Onset Spinal and Bulbar Muscular Atrophy (Kennedy Syndrome): Multiple Cases of Prenatal Testing in a Family.

Christos Yapijakis1,2,3, Achilleas Laskaratos4, Antonia Angelopoulou4, Costas Voumvourakis5.   

Abstract

X-linked spinal and bulbar muscular atrophy (SBMA), also known as Kennedy syndrome, is an adult-onset neurodegenerative disorder characterized by slowly progressive muscle atrophy and other severe symptoms gradually leading to reduced mobility and ultimately to death due to respiratory failure. Two decades ago we reported the first prenatal diagnosis of SBMA worldwide. Here we present a Greek family in which we have performed seven prenatal DNA tests for SBMA mutation after extensive genetic counseling. Since there is not yet a cure for SBMA, prenatal testing may be a good choice for couples at risk for prevention of this neurodegenerative disorder in their offspring. The issues addressed during genetic counseling for such a disabling disorder of adult onset are discussed as a paradigm for other conditions with similar characteristics.

Entities:  

Keywords:  Androgen receptor; Genetic counseling; Kennedy syndrome; Late-onset disorder; Neurodegenerative disease; Prenatal testing; Trinucleotide repeat expansion

Mesh:

Year:  2020        PMID: 32468478     DOI: 10.1007/978-3-030-32633-3_28

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  10 in total

1.  Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

Authors:  A R La Spada; E M Wilson; D B Lubahn; A E Harding; K H Fischbeck
Journal:  Nature       Date:  1991-07-04       Impact factor: 49.962

2.  X-linked spinal and bulbar muscular atrophy of late onset. A separate type of motor neuron disease?

Authors:  C Stefanis; T h Papapetropoulos; S Scarpalezos; G Lygidakis; C P Panayiotopoulos
Journal:  J Neurol Sci       Date:  1975-04       Impact factor: 3.181

3.  Hippocrates of Kos, the father of clinical medicine, and Asclepiades of Bithynia, the father of molecular medicine. Review.

Authors:  Christos Yapijakis
Journal:  In Vivo       Date:  2009 Jul-Aug       Impact factor: 2.155

4.  Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait.

Authors:  W R Kennedy; M Alter; J H Sung
Journal:  Neurology       Date:  1968-07       Impact factor: 9.910

5.  Prenatal diagnosis of X-linked spinal and bulbar muscular atrophy in a Greek family.

Authors:  C Yapijakis; E Kapaki; M Boussiou; D Vassilopoulos; C Papageorgiou
Journal:  Prenat Diagn       Date:  1996-03       Impact factor: 3.050

6.  Preimplantation genetic diagnosis for spinal and bulbar muscular atrophy (SBMA).

Authors:  I Georgiou; K Sermon; W Lissens; A De Vos; P Platteau; D Lolis; A Van Steirteghem; I Liebaers
Journal:  Hum Genet       Date:  2001-06       Impact factor: 4.132

Review 7.  Bulbar and spinal muscular atrophy (Kennedy's disease): a review.

Authors:  J Finsterer
Journal:  Eur J Neurol       Date:  2009-05       Impact factor: 6.089

8.  Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissues.

Authors:  K B Jedele; D Wahl; S Chahrokh-Zadeh; A Wirtz; J Murken; E Holinski-Feder
Journal:  Clin Genet       Date:  1998-08       Impact factor: 4.438

9.  Mechanisms mediating spinal and bulbar muscular atrophy: investigations into polyglutamine-expanded androgen receptor function and dysfunction.

Authors:  Lenore K Beitel; Carlos Alvarado; Shaza Mokhtar; Miltiadis Paliouras; Mark Trifiro
Journal:  Front Neurol       Date:  2013-05-15       Impact factor: 4.003

10.  Correlation of clinical and molecular features in spinal bulbar muscular atrophy.

Authors:  Pietro Fratta; Niranjanan Nirmalananthan; Luc Masset; Iwona Skorupinska; Toby Collins; Andrea Cortese; Sally Pemble; Andrea Malaspina; Elizabeth M C Fisher; Linda Greensmith; Michael G Hanna
Journal:  Neurology       Date:  2014-05-09       Impact factor: 9.910

  10 in total

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