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Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system.
J Am Soc Nephrol. 2006 Aug; 17(8):2253-63.JA

Abstract

Renal tubular dysgenesis is a clinical disorder that is observed in fetuses and characterized by the absence or poor development of proximal tubules, early onset and persistent oligohydramnios that leads to the Potter sequence, and skull ossification defects. It may be acquired during fetal development or inherited as an autosomal recessive disease. It was shown recently that autosomal recessive renal tubular dysgenesis is genetically heterogeneous and linked to mutations in the genes that encode components of the renin-angiotensin system. This study analyzed the clinical expression of the disease in 29 fetus/neonates from 18 unrelated families and evaluated changes in renal morphology and expression of the renin-angiotensin system. The disease was uniformly severe, with perinatal death in all cases as a result of persistent anuria and hypoxia related to pulmonary hypoplasia. Severe defects in proximal tubules were observed in all fetuses from 18 gestational weeks onward, and lesions also involved other tubular segments. They were associated with thickening of the renal arterial vasculature, from the arcuate to the afferent arteries. Renal renin expression was strikingly increased in 19 of 24 patients studied, from 13 families, whereas no renal renin was detected in four patients from three families. Angiotensinogen and angiotensin-converting enzyme were absent or present in only small amounts in the proximal tubule, in correlation with the severity of tubular abnormalities. No specific changes were detected in angiotensin II receptor expression. The severity and the early onset of the clinical and pathologic expression of the disease underline the major importance of this system in fetal kidney function and development in humans. The identification of the disease on the basis of precise histologic analysis and the research of the genetic defect now allow genetic counseling and early prenatal diagnosis.

Authors+Show Affiliations

Institut National de la Santé et de la Recherche Médicale, Unité 574, Collège de France, Paris, France.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

16790508

Citation

Lacoste, Mireille, et al. "Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios: Role of the Renin-Angiotensin System." Journal of the American Society of Nephrology : JASN, vol. 17, no. 8, 2006, pp. 2253-63.
Lacoste M, Cai Y, Guicharnaud L, et al. Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system. J Am Soc Nephrol. 2006;17(8):2253-63.
Lacoste, M., Cai, Y., Guicharnaud, L., Mounier, F., Dumez, Y., Bouvier, R., Dijoud, F., Gonzales, M., Chatten, J., Delezoide, A. L., Daniel, L., Joubert, M., Laurent, N., Aziza, J., Sellami, T., Amar, H. B., Jarnet, C., Frances, A. M., Daïkha-Dahmane, F., ... Gubler, M. C. (2006). Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system. Journal of the American Society of Nephrology : JASN, 17(8), 2253-63.
Lacoste M, et al. Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios: Role of the Renin-Angiotensin System. J Am Soc Nephrol. 2006;17(8):2253-63. PubMed PMID: 16790508.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system. AU - Lacoste,Mireille, AU - Cai,Yi, AU - Guicharnaud,Liliane, AU - Mounier,Françoise, AU - Dumez,Yves, AU - Bouvier,Raymonde, AU - Dijoud,Frédérique, AU - Gonzales,Marie, AU - Chatten,Jane, AU - Delezoide,Anne-Lise, AU - Daniel,Laurent, AU - Joubert,Madeleine, AU - Laurent,Nicole, AU - Aziza,Jacqueline, AU - Sellami,Tahya, AU - Amar,Hatem Ben, AU - Jarnet,Catherine, AU - Frances,Anne Marie, AU - Daïkha-Dahmane,Farida, AU - Coulomb,Aurore, AU - Neuhaus,Thomas J, AU - Foliguet,Bernard, AU - Chenal,Pierre, AU - Marcorelles,Pascale, AU - Gasc,Jean Marie, AU - Corvol,Pierre, AU - Gubler,Marie Claire, Y1 - 2006/06/21/ PY - 2006/6/23/pubmed PY - 2006/12/15/medline PY - 2006/6/23/entrez SP - 2253 EP - 63 JF - Journal of the American Society of Nephrology : JASN JO - J. Am. Soc. Nephrol. VL - 17 IS - 8 N2 - Renal tubular dysgenesis is a clinical disorder that is observed in fetuses and characterized by the absence or poor development of proximal tubules, early onset and persistent oligohydramnios that leads to the Potter sequence, and skull ossification defects. It may be acquired during fetal development or inherited as an autosomal recessive disease. It was shown recently that autosomal recessive renal tubular dysgenesis is genetically heterogeneous and linked to mutations in the genes that encode components of the renin-angiotensin system. This study analyzed the clinical expression of the disease in 29 fetus/neonates from 18 unrelated families and evaluated changes in renal morphology and expression of the renin-angiotensin system. The disease was uniformly severe, with perinatal death in all cases as a result of persistent anuria and hypoxia related to pulmonary hypoplasia. Severe defects in proximal tubules were observed in all fetuses from 18 gestational weeks onward, and lesions also involved other tubular segments. They were associated with thickening of the renal arterial vasculature, from the arcuate to the afferent arteries. Renal renin expression was strikingly increased in 19 of 24 patients studied, from 13 families, whereas no renal renin was detected in four patients from three families. Angiotensinogen and angiotensin-converting enzyme were absent or present in only small amounts in the proximal tubule, in correlation with the severity of tubular abnormalities. No specific changes were detected in angiotensin II receptor expression. The severity and the early onset of the clinical and pathologic expression of the disease underline the major importance of this system in fetal kidney function and development in humans. The identification of the disease on the basis of precise histologic analysis and the research of the genetic defect now allow genetic counseling and early prenatal diagnosis. SN - 1046-6673 UR - https://www.unboundmedicine.com/medline/citation/16790508/Renal_tubular_dysgenesis_a_not_uncommon_autosomal_recessive_disorder_leading_to_oligohydramnios:_Role_of_the_Renin_Angiotensin_system_ L2 - http://jasn.asnjournals.org/cgi/pmidlookup?view=long&pmid=16790508 DB - PRIME DP - Unbound Medicine ER -