Anomalías renales de posición y de fusión

Arrieta, M. Ubetagoyena; Trapote, R. Areses; Lizarraga, D. Arruebarrena

doi:10.1016/j.anpedi.2011.05.011

Cited by 13 publications

(3 citation statements)

References 17 publications

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“…The kidneys originate in the metanephric tissues of the sacral region. [5] During later embryonic developmental stages, the kidneys usually climb to the waist and develop separately from the abdominal wall. Failure to climb into the waist region results in the development of renal ectopia.…”

Section: Discussionmentioning

confidence: 99%

Ectopic immature renal tissue in gubernaculum associated with undescended testis of a 1-year-old child

Bian

Zhang²,

et al. 2017

Medicine

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Section: Discussionmentioning

confidence: 99%

Ectopic immature renal tissue in gubernaculum associated with undescended testis of a 1-year-old child

Bian

Zhang²,

et al. 2017

Medicine

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“…The study including 84 patients with kidney position and fusion anomalies have reported that 21 (25.4%) of these patients also had extra-renal pathology such as skeletal, genital and cardiac anomalies, digestive disease, facial malformations and endocrine disorders. As a result, renal-urinary anomalies and structural extra-renal malformations must be evaluated when renal ectopia or horseshoe kidney is diagnosed [4]. …”

Section: Discussionmentioning

confidence: 99%

A Case with Mega Cisterna Magna Renal and Ear Anomalies: Is This a New Syndrome?

Konca

Caliskan

Taş

2013

Case Reports in Medicine

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Background. Extrarenal pathologies may be associated with renal position and fusion anomalies. According to the literature, our patient is the first horseshoe kidney case that had mega cisterna magna, arachnodactyly, and mild mental retardation. Case Report. A 9-year-old boy admitted because of the myoclonic jerks. He had a dysmorphic face, low-set and cup-shaped ears, arachnodactyly, and mild mental retardation. The patient's laboratory findings were normal except for a mild leucocytosis and hypochromic microcytic anemia. His cerebrospinal fluid was cytologically and biochemically normal. Cranial MRI revealed 1.5 cm diametered mega cisterna magna in the retrocerebellar region. Although there were no significant epileptical discharges in the electroencephalography, there were slow wave discharges arising from the anterior regions of both hemispheres. Because he had stomachache, abdominal ultrasonography was performed, and horseshoe kidney was determined. Abdominal CT did not reveal any abnormalities except the horseshoe kidney. There were not any cardiac pathologies in echocardiography. He had normal 46XY karyotype and there were no repeated chromosomal derangements, but we could not evaluate for molecular and submicroscopic somatic changes. He was treated with valproic acid and myoclonic jerks did not repeat. Conclusion. We suggest that the presence of these novel findings may represent a newly recognized, separate syndrome.

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“…El control de reflujo se realizó con cistografía isotópica. El estudio DMSA realizado en estos pacientes ya ha sido descrito con detalle en una publicación anterior 9 . Se consideraron DMSA anormales las que presentaban una disminución del tamaño renal o de la función renal diferencial con respecto al riñón contralateral inferior al 40%, hipofunción de algún polo renal, hipocaptaciones focales o difusas del radioisótopo y alteraciones en el contorno renal.…”

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