Renal tubular dysgenesis due to twin-twin transfusion (Q94320): Difference between revisions
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A disgenesia tubular renal devida à síndrome de transfusão entre gêmeos (síndrome da transfusão feto-fetal [STFF]) é uma forma adquirida de disgenesia tubular renal que se desenvolve em fetos de doadores devido ao desvio desigual de fator de crescimento e nutrientes para o rim do receptor e é caracterizada por ausência ou mal desenvolvimento dos túbulos proximais, oligoidrâmnio persistente e consequentemente a sequência de Potter (dismorfismo facial com orelhas grandes e achatadas e com implantação baixa, hipoplasia pulmonar, artrogripose e defeitos de posicionamento dos membros). | |||
| description / en | description / en | ||
Renal tubular dysgenesis due to twin-twin transfusion syndrome (TTTS) is an acquired form of renal tubular dysgenesis that develops in donor fetuses due to the uneven shunting of growth factor and nutrients to the kidney of the recipient and is characterised by absent or poorly developed proximal tubules, persistent oligohydramnios and consequently the Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia, arthrogryposis and limb positioning defects). | |||
Revision as of 09:27, 16 August 2026
Renal tubular dysgenesis due to twin-twin transfusion syndrome (TTTS) is an acquired form of renal tubular dysgenesis that develops in donor fetuses due to the uneven shunting of growth factor and nutrients to the kidney of the recipient and is characterised by absent or poorly developed proximal tubules, persistent oligohydramnios and consequently the Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia, arthrogryposis and limb positioning defects).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_122234138 |
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| English | Renal tubular dysgenesis due to twin-twin transfusion |
Renal tubular dysgenesis due to twin-twin transfusion syndrome (TTTS) is an acquired form of renal tubular dysgenesis that develops in donor fetuses due to the uneven shunting of growth factor and nutrients to the kidney of the recipient and is characterised by absent or poorly developed proximal tubules, persistent oligohydramnios and consequently the Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia, arthrogryposis and limb positioning defects). |
