Literature DB >> 9915472

Genitourinary anomalies in the CHARGE association.

D C Ragan1, A J Casale, R C Rink, M P Cain, D D Weaver.   

Abstract

PURPOSE: We identified the incidence and types of genital and urinary anomalies, and established a plan for evaluating the urinary system in the CHARGE association.
MATERIALS AND METHODS: We retrospectively reviewed the charts of 32 patients in whom the CHARGE association was diagnosed.
RESULTS: Of the 32 patients identified 22 (69%) had genitourinary abnormalities. Genital anomalies, including micropenis, penile agenesis, hypospadias, chordee, cryptorchidism, a bifid scrotum, atresia of the uterus, cervix and vagina, and hypoplastic labia majora, labia minora and clitoris, were present in 18 patients (56%). Of the 24 patients who underwent renal ultrasound 10 (42%) were diagnosed with urinary tract anomalies including a solitary kidney, hydronephrosis, renal hypoplasia and duplex kidneys. Further evaluation revealed vesicoureteral reflux, neurogenic bladder secondary to spinal dysraphism, nephrolithiasis, ureteropelvic junction obstruction and a nonfunctioning upper pole in both duplex kidneys.
CONCLUSIONS: There is a high incidence of genitourinary anomalies in the CHARGE association. Because of this high incidence of anomalies, patients with this condition should undergo a careful genitourinary evaluation, including renal and bladder ultrasound, and voiding cystourethrography screening.

Entities:  

Mesh:

Year:  1999        PMID: 9915472

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


  10 in total

1.  Systemic diagnostic testing in patients with apparently isolated uveal coloboma.

Authors:  Nancy Huynh; Delphine Blain; Tanya Glaser; E Lauren Doss; Wadih M Zein; David M Lang; Eva H Baker; Suvimol Hill; Carmen C Brewer; Jeffrey B Kopp; Tanya M Bardakjian; Irene H Maumenee; Bronwyn J Bateman; Brian P Brooks
Journal:  Am J Ophthalmol       Date:  2013-09-05       Impact factor: 5.258

2.  CHARGE Syndrome.

Authors:  S K Jatana; K Venkatnarayan; Mng Nair
Journal:  Med J Armed Forces India       Date:  2011-07-21

3.  Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

Authors:  D Sanlaville; H C Etchevers; M Gonzales; J Martinovic; M Clément-Ziza; A-L Delezoide; M-C Aubry; A Pelet; S Chemouny; C Cruaud; S Audollent; C Esculpavit; G Goudefroye; C Ozilou; C Fredouille; N Joye; N Morichon-Delvallez; Y Dumez; J Weissenbach; A Munnich; J Amiel; F Encha-Razavi; S Lyonnet; M Vekemans; T Attié-Bitach
Journal:  J Med Genet       Date:  2005-09-16       Impact factor: 6.318

4.  Unique phenotype in a patient with CHARGE syndrome.

Authors:  Shobhit Jain; Hyung-Goo Kim; Felicitas Lacbawan; Irene Meliciani; Wolfgang Wenzel; Ingo Kurth; Josefina Sharma; Morris Schoeneman; Svetlana Ten; Lawrence C Layman; Elka Jacobson-Dickman
Journal:  Int J Pediatr Endocrinol       Date:  2011-10-13

5.  Inappropriate p53 activation during development induces features of CHARGE syndrome.

Authors:  Jeanine L Van Nostrand; Colleen A Brady; Heiyoun Jung; Daniel R Fuentes; Margaret M Kozak; Thomas M Johnson; Chieh-Yu Lin; Chien-Jung Lin; Donald L Swiderski; Hannes Vogel; Jonathan A Bernstein; Tania Attié-Bitach; Ching-Pin Chang; Joanna Wysocka; Donna M Martin; Laura D Attardi
Journal:  Nature       Date:  2014-08-03       Impact factor: 49.962

Review 6.  Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature.

Authors:  Thomas Bjørsum-Meyer; Morten Herlin; Niels Qvist; Michael B Petersen
Journal:  J Med Case Rep       Date:  2016-12-21

Review 7.  Guidelines in CHARGE syndrome and the missing link: Cranial imaging.

Authors:  Christa M de Geus; Rolien H Free; Berit M Verbist; Deborah A Sival; Kim D Blake; Linda C Meiners; Conny M A van Ravenswaaij-Arts
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-11-23       Impact factor: 3.908

8.  Integrated anatomy of the neuromuscular, visceral, vascular, and urinary tissues determined by MRI for a surgical approach to lateral lumbar interbody fusion in the presence or absence of spinal deformity.

Authors:  Shigeto Ebata; Tetsuro Ohba; Hirotaka Haro
Journal:  Spine Surg Relat Res       Date:  2018-02-28

9.  CHARGE syndrome-associated proteins FAM172A and CHD7 influence male sex determination and differentiation through transcriptional and alternative splicing mechanisms.

Authors:  Catherine Bélanger; Tatiana Cardinal; Elizabeth Leduc; Robert S Viger; Nicolas Pilon
Journal:  FASEB J       Date:  2022-03       Impact factor: 5.834

Review 10.  Eyes on CHARGE syndrome: Roles of CHD7 in ocular development.

Authors:  Laura A Krueger; Ann C Morris
Journal:  Front Cell Dev Biol       Date:  2022-09-08
  10 in total

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