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Renal tubular dysgenesis

ORPHA:3033Malformation syndromeAutosomal recessive, Not applicableAntenatal

Фенотипы (13)

Очень частый (80–99%)8
HP:0001382Joint hypermobility
HP:0000114Proximal tubulopathy
HP:0000316Hypertelorism
HP:0001561Polyhydramnios
HP:0001622Premature birth
HP:0002089Pulmonary hypoplasia
HP:0005562Multiple renal cysts
HP:0008660Renotubular dysgenesis
Периодический (5–29%)5
HP:0000112Nephropathy
HP:0000252Microcephaly
HP:0001562Oligohydramnios
HP:0001636Tetralogy of Fallot
HP:0007598Bilateral single transverse palmar creases

Эпидемиология (2)

Point prevalence
Unknown
Worldwide
Prevalence at birth
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы