Literature DB >> 20490649

Birth of a healthy infant following preimplantation PKHD1 haplotyping for autosomal recessive polycystic kidney disease using multiple displacement amplification.

Eduardo C Lau1, Marleen M Janson, Mark R Roesler, Ellis D Avner, Estil Y Strawn, David P Bick.   

Abstract

PURPOSE: To develop a reliable preimplantation genetic diagnosis protocol for couples who both carry a mutant PKHD1 gene wishing to conceive children unaffected with autosomal recessive polycystic kidney disease (ARPKD).
METHODS: Development of a unique protocol for preimplantation genetic testing using whole genome amplification of single blastomeres by multiple displacement amplification (MDA), and haplotype analysis with novel short tandem repeat (STR) markers from the PKHD1 gene and flanking sequences, and a case report of successful utilization of the protocol followed by successful IVF resulting in the birth of an infant unaffected with ARPKD.
RESULTS: We have developed 20 polymorphic STR markers suitable for linkage analysis of ARPKD. These linked STR markers have enabled unambiguous identification of the PKHD1 haplotypes of embryos produced by at-risk couples.
CONCLUSIONS: We have developed a reliable protocol for preimplantation genetic diagnosis of ARPKD using single-cell MDA products for PKHD1 haplotyping.

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Year:  2010        PMID: 20490649      PMCID: PMC2922704          DOI: 10.1007/s10815-010-9432-5

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  46 in total

1.  Determination of the genetic status of cleavage-stage human embryos by microsatellite marker analysis following multiple displacement amplification.

Authors:  Pamela J Renwick; Cathryn M Lewis; Stephen Abbs; Caroline Mackie Ogilvie
Journal:  Prenat Diagn       Date:  2007-03       Impact factor: 3.050

2.  Improved multiple displacement amplification with phi29 DNA polymerase for genotyping of single human cells.

Authors:  Gyanendra Kumar; Elena Garnova; Michael Reagin; Andrea Vidali
Journal:  Biotechniques       Date:  2008-06       Impact factor: 1.993

Review 3.  Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD).

Authors:  William E Sweeney; Ellis D Avner
Journal:  Cell Tissue Res       Date:  2006-06-10       Impact factor: 5.249

4.  Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification.

Authors:  Zi Ren; Canquan Zhou; Yanwen Xu; Jie Deng; Haitao Zeng; Yanhong Zeng
Journal:  Mol Hum Reprod       Date:  2007-04-16       Impact factor: 4.025

5.  Preimplantation HLA haplotyping using tri-, tetra-, and pentanucleotide short tandem repeats for HLA matching.

Authors:  Sarah L Bick; David P Bick; Brent E Wells; Mark R Roesler; Estil Y Strawn; Eduardo C Lau
Journal:  J Assist Reprod Genet       Date:  2008-08-02       Impact factor: 3.412

6.  Preimplantation genetic diagnosis of X-linked retinoschisis.

Authors:  Belén Lledó; Jorge Ten; Dori Rodriguez-Arnedo; Joaquín Llácer; Rafael Bernabeu
Journal:  Reprod Biomed Online       Date:  2008-06       Impact factor: 3.828

7.  Delivery of a normal baby after preimplantation genetic diagnosis for non-ketotic hyperglycinaemia.

Authors:  Ali Hellani; Aref Sammour; Lars Johansson; Abdulssamad El-Sheikh
Journal:  Reprod Biomed Online       Date:  2008-06       Impact factor: 3.828

Review 8.  Preimplantation genetic diagnosis: technology and clinical applications.

Authors:  Amy Swanson; Estil Strawn; Eduardo Lau; David Bick
Journal:  WMJ       Date:  2007-05

9.  Preimplantation genetic diagnosis for autosomal recessive polycystic kidney disease.

Authors:  N Gigarel; N Frydman; P Burlet; V Kerbrat; G Tachdjian; R Fanchin; C Antignac; R Frydman; A Munnich; J Steffann
Journal:  Reprod Biomed Online       Date:  2008-01       Impact factor: 3.828

10.  Primase-based whole genome amplification.

Authors:  Ying Li; Hyun-Jin Kim; Chunyang Zheng; Wing Huen A Chow; Jeonghwa Lim; Brendan Keenan; Xiaojing Pan; Bertrand Lemieux; Huimin Kong
Journal:  Nucleic Acids Res       Date:  2008-06-17       Impact factor: 16.971

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  12 in total

Review 1.  Diagnosis and management of childhood polycystic kidney disease.

Authors:  William E Sweeney; Ellis D Avner
Journal:  Pediatr Nephrol       Date:  2010-10-29       Impact factor: 3.714

2.  Preimplantation genetic diagnosis for α-and β-double thalassemia.

Authors:  Xiaoting Shen; Yanwen Xu; Yiping Zhong; Canquan Zhou; Yanhong Zeng; Guanglun Zhuang; Chenhui Ding; Tao Li
Journal:  J Assist Reprod Genet       Date:  2011-06-11       Impact factor: 3.412

Review 3.  Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects.

Authors:  Erum A Hartung; Lisa M Guay-Woodford
Journal:  Pediatrics       Date:  2014-08-11       Impact factor: 7.124

4.  An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screening.

Authors:  Li-Jung Chang; Shee-Uan Chen; Yi-Yi Tsai; Chia-Cheng Hung; Mei-Ya Fang; Yi-Ning Su; Yu-Shih Yang
Journal:  Clin Exp Reprod Med       Date:  2011-09-30

Review 5.  Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy.

Authors:  William E Sweeney; Ellis D Avner
Journal:  Pediatr Res       Date:  2013-10-31       Impact factor: 3.756

6.  Novel Mutation in the PKHD1 Gene Diagnosed Prenatally in a Fetus with Autosomal Recessive Polycystic Kidney Disease.

Authors:  Pankaj Thakur; Paul Speer; Aleksandar Rajkovic
Journal:  Case Rep Genet       Date:  2014-07-13

Review 7.  Emerging Therapies for Childhood Polycystic Kidney Disease.

Authors:  William E Sweeney; Ellis D Avner
Journal:  Front Pediatr       Date:  2017-04-19       Impact factor: 3.418

8.  Preimplantation Genetic Testing for Monogenic Kidney Disease.

Authors:  Rozemarijn Snoek; Marijn F Stokman; Klaske D Lichtenbelt; Theodora C van Tilborg; Cindy E Simcox; Aimée D C Paulussen; Jos C M F Dreesen; Franka van Reekum; A Titia Lely; Nine V A M Knoers; Christine E M de Die-Smulders; Albertien M van Eerde
Journal:  Clin J Am Soc Nephrol       Date:  2020-08-27       Impact factor: 8.237

9.  Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney disease.

Authors:  Jun Miyazaki; Mayuko Ito; Haruki Nishizawa; Takema Kato; Yukito Minami; Hidehito Inagaki; Tamae Ohye; Masafumi Miyata; Hiroko Boda; Yuka Kiriyama; Makoto Kuroda; Takao Sekiya; Hiroki Kurahashi; Takuma Fujii
Journal:  BMC Med Genet       Date:  2015-10-26       Impact factor: 2.103

10.  Preimplantation Genetic Testing for Monogenic Disease of Spinal Muscular Atrophy by Multiple Displacement Amplification: 11 unaffected livebirths.

Authors:  Yu Fu; Xiaoting Shen; Haitao Wu; Dongjia Chen; Canquan Zhou
Journal:  Int J Med Sci       Date:  2019-09-07       Impact factor: 3.738

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