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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A study of 15 patients. This can be due to chance, environment, or genetics. National Center for Biotechnology InformationU.

The sindrome de potter is often small, nondistensible and may be filled with a minute amount of fluid. Magnetic resonance imaging diagnosis of severe fetal renal anomalies. There are those in the medical and research fields that use the term Potter sequence to specifically refer to only cases of BRA, while other groups use the term to loosely refer to all instances of oligohydramnios and anhydramnios regardless of the specific cause.

Sindrome de potter failed induction will thereby cause the subsequent degeneration sindrrome the metanephros by apoptosis and other mechanisms. Fras1, a basement membrane-associated protein mutated in Fraser syndrome, mediates both the initiation of the mammalian kidney and the integrity of renal glomeruli.


Síndrome de Potter by Catalina Pino on Prezi

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Bilateral renal agenesis was seen in 95 cases sindrome de potter out of this prenatal diagnosis was made in 86 cases [ 32 ].

HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.

Potter’s Sequence

Angiotensin-II-receptor sindrome de potter in pregnancy. Cardiovascular malformations associated with congenital anomalies of the urinary system.

Physical examination revealed the presence of a palpable mass in the right flank and hypogastrium. Mutation of the formin IV gene leads only to kidney abnormalities. In one other study from Europe’s 17 registries reported cases diagnosed with 11 severe congenital malformations, out sindrome de potter which cases had bilateral renal agenesis [ 33 ]. Open in a separate window.

Potter sequence

Optteror “Mermaid syndrome” which occurs approximately in 1: Pathophysiology Prior to 16 weeks’ gestations, the amount of amniotic fluid is dependent on the transmembrane flow. At sindrome de potter, hypoglycemic episodes were characterized. This article has been cited by other articles in PMC. On autopsy, the following findings were noted. Sindrme is more accurately described as a “sequence” or chain of events that may have different beginnings absent kidneyscystic kidneysobstructed ureters or other causesbut which all end with the same conclusion absent or reduced volume sindrome de potter amniotic fluid.


Ximena Concha Paula Soto.

Potter Syndrome: Background, Pathophysiology, Epidemiology

The resulting oligohydramnios is the cause of the deformities in Potter’s sequence. Hnf1b and Pax2 cooperate to control different pathways in kidney and ureter morphogenesis.

The term Potter syndrome is most frequently associated with sindrome de potter condition of oligohydramnios sequence regardless of the root cause of the absence or reduced volume of amniotic fluid.

Babies born with this condition are either still born or die very early within the neonatal period.

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The frequency of other causes sindrome de potter Potter syndrome is not known. Potter’s sequence is a rare fatal disorder that occurs in sporadic and autosomal sindrome de potter forms with an incidence of 1 in births. GLI3 repressor controls nephron pottef via regulation of Wnt11 and Ret in ureteric tip cells. A male, year-old patient admitted because of a progressive increase of the abdominal volume for five months, in association with daily episodes of sudden sweating with syncope.