Keywords: Potter facies, pulmonary hypoplasia, renal agenesis terminology as all cases of this syndrome do not have exactly the same set of signs, but they. Síndrome de Doege-Potter by non-islet cell tumors), Doege-Potter syndrome ( DPS) was considered as the Tumor fibroso solitário do rim: descrição de caso. 16 Oct Transcript of Síndrome de Potter. P Paciente neonatal con riñón multiquístico. I Nefrectomía C Tratamiento expectante. O Menor nivel de.

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Potter’s Sequence

Urachal cyst Urachal fistula Urachal sinus. Heterozygotes may have a unilateral renal abnormality while the contralateral kidney has normal development [ 7 ]. The fetus continuously swallows amniotic fluid, which is reabsorbed by the gastrointestinal tract and then reintroduced into the amniotic cavity by the kidneys via urination. It can be caused by renal diseases such as bilateral renal agenesis BRAatresia of the ureter or urethra causing obstruction of the urinary tract, polycystic or multicystic kidney diseases, renal hypoplasia, amniotic rupturetoxemia, or uteroplacental insufficiency from maternal hypertension.

Urology Annals, 6, Do you really want to delete this prezi? Not to be confused with Doege—Potter syndrome or Pott’s disease. Observations in a series of infants and children with urinary system malformations. The Turkish Journal of Pediatrics, 56, The role of the pediatric surgeon in the perinatal multidisciplinary team.

Sindrome de potter 16 survivors have chronic kidney disease, with sindrome de potter developing end stage renal failure median sindrome de potter 0. Newborn male babies have an increased incidence of the Potter’s sequence because they have a higher rate of Eagle—Barrett Prune belly syndrome and obstructive uropathy secondary to posterior urethral valves.


Epispadias Hypospadias Posterior urethral valves.

The condition has been reported to occur twice as commonly in males as in females, suggesting that certain genes of the Y chromosome may act as modifiers. However, no candidate genes sindrome de potter the Y chromosome have yet been identified. Share cases and questions with Physicians on Medscape consult.

Potter’s Sequence

Physical examination revealed the presence of a palpable mass in the right flank and hypogastrium. Am J Med Genet A. Regular follow-up and antenatal checkup should be done to diagnose oligohydramnios to sindrpme the complications resulting from it.

The influence of the intrauterine environment in the causation of sindrome de potter postural deformities, with special reference to congenital dislocation of the hip. This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3. Kolteand Panduranga R. Neonates with the milder form of Potter syndrome have an increased morbidity rate because of respiratory failuresindrome de potterand acute renal failure during the neonatal period.

Potter sequence is the atypical physical appearance of a baby due to oligohydramnios experienced when in the uterus. Masa Abdominal en estudio.

Solitary fibrous tumors of the soft tissues: Histopathological and immunohistochemical analyzes are necessary to confirm the diagnosis 6. Potter’s sequence sindrome de potter first described by Edith Potter in Magnetic resonance imaging diagnosis of severe fetal renal anomalies. Decrease in the pktter of amniotic fluid may be due to decreased urine production secondary to bilateral renal agenesis, obstruction to the urinary tract, or occasionally prolonged rupture of membranes.


Bilateral renal sindrome de potter BRA was first recognized as a defect of porter fetal development in by Wolfstrigel. Neither calcification nor fat were observed.

Other anomalies of the classic Potter sequence infant include a parrot beak nose, redundant skin, and the most common characteristic of infants with BRA which is a skin fold of tissue extending from the medial canthus across the cheek.

Congenital malformations and deformations of urinary system Q60—Q64 Males have an increased incidence of the Potter syndrome because they have a higher rate of Eagle-Barrett prune belly syndrome [ 40 ] and obstructive uropathy secondary to posterior urethral valves.

Support Center Support Center. Pediatr Surg Int, 27, — The associated maternal high-risk factors for bilateral renal agenesis are sindrome de potter body mass index sindrome de potter than 30, smoking, and binge drinking.

Umbilical cord showed only two vessels composed of single umbilical artery [ Figure 3a ]. The clinical significance of an empty renal fossa on prenatal sonography. sindrome de potter

This may be due to decreased urine production secondary to bilateral renal agenesis, obstruction of the urinary tract, or, occasionally, prolonged rupture of membranes [ 23 ]. Multiple congenital ocular anomalies with bilateral agenesis sindrome de potter the urinary tract. See more popular or the latest prezis.

Brain defects in infants with Potter syndrome oligohydramnios sequence. Additionally, candidate genetic pathways would be expected to involve genes expressed in the developing urogenital system UGS.