Literature DB >> 12441983

Genitourinary malformations in chromosome 22q11.2 deletion.

Hsi-Yang Wu1, Susan L Rusnack, Richard D Bellah, Natalie Plachter, Donna M McDonald-McGinn, Elaine H Zackai, Douglas A Canning.   

Abstract

PURPOSE: We reviewed our experience with genitourinary malformations associated with chromosome 22q11.2 deletion.
MATERIALS AND METHODS: We retrospectively reviewed patient intake charts at the 22q clinic at our institution. We assessed 73 renal/bladder ultrasounds and 7 autopsies performed between 1998 and 2000 for renal and bladder malformations. A total of 149 male patients were evaluated for possible testicular and urethral malformations.
RESULTS: Of 80 patients 25 (31%) had a structural urinary tract anomaly. Another 8 patients had renal agenesis or multicystic dysplastic kidney, 4 had hydronephrosis and 5 had vesicoureteral reflux or an irregular bladder, while 8 of 73 (11%) had dysfunctional voiding, 9 of 149 (6%) had undescended testes and 12 of 149 (8%) had hypospadias.
CONCLUSIONS: Screening renal/bladder ultrasound, careful voiding history and medical but not surgical therapy are recommended for renal and bladder anomalies associated with 22q11.2 deletion. The need for surgery for cryptorchidism and hypospadias is slightly higher than in the general population.

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Mesh:

Year:  2002        PMID: 12441983     DOI: 10.1097/01.ju.0000032176.07703.23

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  12 in total

1.  Primary amenorrhea and absent uterus in the 22q11.2 deletion syndrome.

Authors:  Usha T Sundaram; Donna M McDonald-McGinn; Dale Huff; Beverly S Emanuel; Elaine H Zackai; Deborah A Driscoll; Joann Bodurtha
Journal:  Am J Med Genet A       Date:  2007-09-01       Impact factor: 2.802

2.  Anomalies of the genitourinary tract in children with 22q11.2 deletion syndrome.

Authors:  Jason P Van Batavia; Terrence B Crowley; Evanette Burrows; Elaine H Zackai; Simone Sanna-Cherchi; Donna M McDonald-McGinn; Thomas F Kolon
Journal:  Am J Med Genet A       Date:  2018-12-24       Impact factor: 2.802

3.  Microarray analysis in pregnancies with isolated unilateral kidney agenesis.

Authors:  Lena Sagi-Dain; Idit Maya; Amir Peleg; Adi Reches; Ehud Banne; Hagit N Baris; Tamar Tenne; Amihood Singer; Shay Ben-Shachar
Journal:  Pediatr Res       Date:  2018-02-07       Impact factor: 3.756

4.  Presenting phenotype in 100 children with the 22q11 deletion syndrome.

Authors:  Sólveig Oskarsdóttir; Christina Persson; Bengt O Eriksson; Anders Fasth
Journal:  Eur J Pediatr       Date:  2004-11-23       Impact factor: 3.183

5.  Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.

Authors:  Esther Lopez-Rivera; Yangfan P Liu; Miguel Verbitsky; Blair R Anderson; Valentina P Capone; Edgar A Otto; Zhonghai Yan; Adele Mitrotti; Jeremiah Martino; Nicholas J Steers; David A Fasel; Katarina Vukojevic; Rong Deng; Silvia E Racedo; Qingxue Liu; Max Werth; Rik Westland; Asaf Vivante; Gabriel S Makar; Monica Bodria; Matthew G Sampson; Christopher E Gillies; Virginia Vega-Warner; Mariarosa Maiorana; Donald S Petrey; Barry Honig; Vladimir J Lozanovski; Rémi Salomon; Laurence Heidet; Wassila Carpentier; Dominique Gaillard; Alba Carrea; Loreto Gesualdo; Daniele Cusi; Claudia Izzi; Francesco Scolari; Joanna A E van Wijk; Adela Arapovic; Mirna Saraga-Babic; Marijan Saraga; Nenad Kunac; Ali Samii; Donna M McDonald-McGinn; Terrence B Crowley; Elaine H Zackai; Dorota Drozdz; Monika Miklaszewska; Marcin Tkaczyk; Przemyslaw Sikora; Maria Szczepanska; Malgorzata Mizerska-Wasiak; Grazyna Krzemien; Agnieszka Szmigielska; Marcin Zaniew; John M Darlow; Prem Puri; David Barton; Emilio Casolari; Susan L Furth; Bradley A Warady; Zoran Gucev; Hakon Hakonarson; Hana Flogelova; Velibor Tasic; Anna Latos-Bielenska; Anna Materna-Kiryluk; Landino Allegri; Craig S Wong; Iain A Drummond; Vivette D'Agati; Akira Imamoto; Jonathan M Barasch; Friedhelm Hildebrandt; Krzysztof Kiryluk; Richard P Lifton; Bernice E Morrow; Cecile Jeanpierre; Virginia E Papaioannou; Gian Marco Ghiggeri; Ali G Gharavi; Nicholas Katsanis; Simone Sanna-Cherchi
Journal:  N Engl J Med       Date:  2017-01-25       Impact factor: 91.245

Review 6.  Hypospadias: A Comprehensive Review Including Its Embryology, Etiology and Surgical Techniques.

Authors:  Sattam A Halaseh; Shahed Halaseh; Mohannad Ashour
Journal:  Cureus       Date:  2022-07-31

7.  Murine model indicates 22q11.2 signaling adaptor CRKL is a dosage-sensitive regulator of genitourinary development.

Authors:  Meade Haller; Qianxing Mo; Akira Imamoto; Dolores J Lamb
Journal:  Proc Natl Acad Sci U S A       Date:  2017-04-24       Impact factor: 11.205

Review 8.  22q11.2 deletion syndrome.

Authors:  Donna M McDonald-McGinn; Kathleen E Sullivan; Bruno Marino; Nicole Philip; Ann Swillen; Jacob A S Vorstman; Elaine H Zackai; Beverly S Emanuel; Joris R Vermeesch; Bernice E Morrow; Peter J Scambler; Anne S Bassett
Journal:  Nat Rev Dis Primers       Date:  2015-11-19       Impact factor: 52.329

9.  Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2.

Authors:  M Cristina Digilio; Donna M McDonald-McGinn; Carrie Heike; Charles Catania; Bruno Dallapiccola; Bruno Marino; Elaine H Zackai
Journal:  Am J Med Genet A       Date:  2009-12       Impact factor: 2.802

10.  Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

Authors:  Miguel Verbitsky; Priya Krithivasan; Ekaterina Batourina; Atlas Khan; Sarah E Graham; Maddalena Marasà; Hyunwoo Kim; Tze Y Lim; Patricia L Weng; Elena Sánchez-Rodríguez; Adele Mitrotti; Dina F Ahram; Francesca Zanoni; David A Fasel; Rik Westland; Matthew G Sampson; Jun Y Zhang; Monica Bodria; Byum Hee Kil; Shirlee Shril; Loreto Gesualdo; Fabio Torri; Francesco Scolari; Claudia Izzi; Joanna A E van Wijk; Marijan Saraga; Domenico Santoro; Giovanni Conti; David E Barton; Mark G Dobson; Prem Puri; Susan L Furth; Bradley A Warady; Isabella Pisani; Enrico Fiaccadori; Landino Allegri; Maria Ludovica Degl'Innocenti; Giorgio Piaggio; Shumyle Alam; Maddalena Gigante; Gianluigi Zaza; Pasquale Esposito; Fangming Lin; Ana Cristina Simões-E-Silva; Andrzej Brodkiewicz; Dorota Drozdz; Katarzyna Zachwieja; Monika Miklaszewska; Maria Szczepanska; Piotr Adamczyk; Marcin Tkaczyk; Daria Tomczyk; Przemyslaw Sikora; Malgorzata Mizerska-Wasiak; Grazyna Krzemien; Agnieszka Szmigielska; Marcin Zaniew; Vladimir J Lozanovski; Zoran Gucev; Iuliana Ionita-Laza; Ian B Stanaway; David R Crosslin; Craig S Wong; Friedhelm Hildebrandt; Jonathan Barasch; Eimear E Kenny; Ruth J F Loos; Brynn Levy; Gian Marco Ghiggeri; Hakon Hakonarson; Anna Latos-Bieleńska; Anna Materna-Kiryluk; John M Darlow; Velibor Tasic; Cristen Willer; Krzysztof Kiryluk; Simone Sanna-Cherchi; Cathy L Mendelsohn; Ali G Gharavi
Journal:  J Am Soc Nephrol       Date:  2021-02-17       Impact factor: 14.978

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