Séquence de Potter


Séquence de Potter

La séquence (ou le syndrome) de Potter est une série de malformations caractéristiques du nouveau-né suite à un oligo-hydramnios.

Caractéristiques

Elle se caractérise par une agénésie rénale (qui cause l’oligo-hydramnios), un faciès typique et des malformations des quatre membres.


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  • Potter syndrome — DiseaseDisorder infobox Name = Potter syndrome ICD10 = ICD10|Q|60|6|q|60 ICD9 = ICD9|753.0, ICD9|658.0, ICD9|761.2 (for oligohydramnios) ICDO = Caption = OMIM = MedlinePlus = 001268 eMedicineSubj = ped eMedicineTopic = 1878 DiseasesDB = 11252… …   Wikipedia

  • Potter sequence — Not to be confused with Doege Potter syndrome or Pott s Disease. Potter sequence Classification and external resources ICD 10 Q60.6 ICD 9 …   Wikipedia

  • Potter facies syndrome — Pot·ter facies, syndrome (potґər) [Edith Louise Potter, American physician, 1901–1993] see under facies and see oligohydramnios sequence, under sequence …   Medical dictionary

  • Potter syndrome — a congenital condition characterized by absence of kidneys, resulting in decreased amniotic fluid (see oligohydramnios) and compression of the fetus. Babies have poorly developed lungs, a characteristic wrinkled and flattened facial appearance,… …   Medical dictionary

  • Potter facies — the characteristic facial appearance seen with oligohydramnios sequence (see under sequence), consisting of a flattened nose, receding chin, wide interpupillary space, large low set ears, and sometimes other anomalies …   Medical dictionary

  • Doege-Potter syndrome — Not to be confused with Potter sequence. Doege Potter syndrome Classification and external resources The structure of IGF 2, responsible for the hypoglycemia associated with Doege Potter syndrome Doege Potter syndrome (DPS) is a …   Wikipedia

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