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Renale Hypodysplasie/Aplasie 1

Die renale Aplasie 1 ist eine schwere Form der Fehlbildungen im Urogentialbereich (CAKUT). Das Spektrum reicht von bilateraler Aplasie (meist letal) über unilaterale Aplasie mit kontralateraler Hyposdysplasie bis hin zu den schweren angeborenen Obstruktionen im Harntrakt. In den verantwortlichen Genen können ein (dominant) oder zwei (rezessiv) Allele betroffen sein.

Symptome

Nierenfehlbildungen
Die schweren Fehlbildungen bei Nierenaplasie Typ 1 sind oft lebensbedrohlich.

Gliederung

Renale Hypodysplasie/Aplasie
GREB1L
Renale Hypodysplasie/Aplasie 1
DSTYK
ITGA8
PAX2
RET
UPK3A
Renale Hypodysplasie/Aplasie 2

Referenzen:

1.

Müller U et al. (1997) Integrin alpha8beta1 is critically important for epithelial-mesenchymal interactions during kidney morphogenesis.

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2.

Selig AM et al. (1993) Renal dysplasia, megalocystis, and sirenomelia in four siblings.

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3.

Scott RJ et al. (1995) Potter's syndrome in the second trimester--prenatal screening and pathological findings in 60 cases of oligohydramnios sequence.

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4.

Schinzel A et al. (1978) Bilateral renal agenesis in 2 male sibs born to consanguineous parents.

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5.

Monn E et al. (1984) Hereditary renal adysplasia.

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6.

Roodhooft AM et al. (1984) Familial nature of congenital absence and severe dysgenesis of both kidneys.

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7.

Yates JR et al. (1984) Concordant monozygotic twins with bilateral renal agenesis.

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8.

Winter JS et al. (1968) A familial syndrome of renal, genital, and middle ear anomalies.

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9.

Rizza JM et al. (1971) Bilateral renal agenesis in two female siblings.

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10.

Hack M et al. (1974) Familial aggregation in bilateral renal agenesis.

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11.

Kohn G et al. (1973) The association of bilateral and unilateral renal aplasia in the same family.

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12.

Carter CO et al. (1979) A family study of renal agenesis.

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13.

Cain DR et al. (1974) Familial renal agenesis and total dysplasia.

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14.

Wilson RD et al. (1985) Renal agenesis in British Columbia.

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15.

Bankier A et al. (1985) A pedigree study of perinatally lethal renal disease.

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16.

Morse RP et al. (1987) Bilateral renal agenesis in three consecutive siblings.

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17.

Bankier A et al. (1988) Renal ultrasound examination of parents in dominantly inherited renal adysplasia--a note of caution.

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18.

Sanna-Cherchi S et al. (2012) Copy-number disorders are a common cause of congenital kidney malformations.

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19.

None (1946) Facial characteristics of infants with bilateral renal agenesis.

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20.

DAVIDSON WM et al. (1954) Bilateral absence of the kidneys and related congenital anomalies.

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21.

BAIN AD et al. (1964) NEWBORN AFTER PROLONGED LEAKAGE OF LIQUOR AMNII.

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22.

None (1954) Bilateral agenesis of the kidneys in two consecutive infants.

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23.

Joss S et al. (2003) De novo translocation (1; 2)(q32; p25) associated with bilateral renal dysplasia.

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24.

Ogata T et al. (2000) Genetic evidence for a novel gene(s) involved in urogenital development on 10q26.

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25.

Buchta RM et al. (1973) Familial bilateral renal agenesis and hereditary renal adysplasia.

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26.

Schmidt W et al. (1982) Genetics, pathoanatomy and prenatal diagnosis of Potter I syndrome and other urogenital tract diseases.

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27.

Humbert C et al. (2014) Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans.

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28.

OMIM.ORG article

Omim 191830 external link
Update: 14. August 2020
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