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Prune belly sendromu ve at nalı böbrek birlikteliği (olgu sunumu)

Association of Prune belly syndrome and horse shoe kidney (case report)

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Abstract (2. Language): 
A male fetus with a gestational age of 15 weeks with abdominal muscular and umbilical cord vessel anomalies in addition to urinary system anomalies is presented in this article. The association of Prune belly syndrome characterized with urinary system anomalies and abdominal muscular hypoplasia/agenesis with multicystic renal dysplasia is well known. This case is presented because the association of horse shoe kidney with this syndrome has not been reported before.
Abstract (Original Language): 
Bu makalede üriner sistem anomalilerinin yanı sıra abdominal kas ve umbilikal arter anomalisi olan 15 haftalık bir erkek fetus sunulmaktadır. Üriner sistem anomalileri ve abdominal kasların hipoplazisi/agenezisi ile karakterize Prune belly sendromunun multikistik renal displazi ile birlikteliği bilinmektedir. Olgu, bu sendrom ile at nalı böbrek birlikteliğinin bildirilmemiş olması nedeniyle sunulmaktadır.
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REFERENCES

References: 

Kaynaklar
1. Volmar KE, Fritsch KM, Perlman EJ, Hutchins GM.
Patterns of congenital lower urinary tract obstructive
uropathy: relation to abnormal prostate and bladder
development and the prune belly syndrome. Pediatr
Dev Pathol 2001; 4: 467-472.
2. Cazorla E, Ruiz F, Abad A, Monleon J. Prune belly
syndrome: early antenatal diagnosis. Eur J Obstet
Gynecol Reprod Biol 1997; 72: 31-33.
3. Friedmann W, Vogel M, Dimer JS, Luttkus UB,
Dudenhausen JW. Perinatal differential diagnosis of
cystic kidney disease and urinary tract obstruction:
anatomic pathologic ultrasonographic and genetic
findings. Eur J Obstet Gynecol Reprod Biol 2000; 89:
127-133.
4. Kumar S, Fisk NM. Distal urinary obstruction. Clin
Perinatol 2003; 30: 507-519.
5. Guillen DR, Lowichik A, Schneider NR, Cohen DS,
Garcia S, Zinn AR. Prune belly syndrome and other
anomalies in a stillborn fetus with a ring X chromosome
lacking XIST. Am J Med Genet 1997; 70: 32-36.
6. Cromie WJ. Implications of antenatal ultrasound
screening in the incidence of major genitourinary
malformations. Semin Pediatr Surg 2001; 10: 204-211.
7. Tunca Y, Oğur G, Başer I, et al. Fetal ultrasound
abnormalities in 108 pregnancies: correlation with
fetal karyotype autopsy findings, radiologic findings
and postnatal outcome. Gülhane Tıp Dergisi 1998; 40:
455-465.
8. Tunca Y, İmirzalıoğlu N, Güran Ş, et al. The importance
of multidisciplinary prenatal and postnatal evaluation in
a case with VACTERL association in genetic counselling
for following pregnancy. Gülhane Tıp Dergisi 1998; 40:
483-486.

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