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The malformations of the urinary system in autosomal disorders

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Summary

Data from the world literature about the pathology of the urinary system in autosomal chromosomal disorders are analyzed and compared with our own morphological investigations of this system in 63 cases of chromosomal disorders (Patau's, Edwards', Down's, Orbeli's, Wolf-Hirschhorn's syndromes, partial trisomy B and inversion of chromosome 2). The urinary system is most frequently involved in “cat-eye”, triploidy, Orbeli's, Patau's and Edwards' syndromes. All known malformations of the urinary system are observed in children with chromosomal diseases, except infantile polycystic kidney and medullary “sponge” kidney. The authors recognize specific and nonspecific abnormalities of the urinary system. Nonspecific abnormalities, as simple renal dysgenesis, may be observed in all chromosomal disorders. Specific abnormalities are found only in certain chromosomal diseases. These malformations are an excess of embryonal lobulation of the kidney with the increase of its weight and cystic changes (Patau's syndrome), crossed renal ectopy with fusion and horseshoe kidney (Edwards' syndrome), unilateral renal agenesis (Orbeli's syndrome), hypospadia (Wolf-Hirschhorn's syndrome). A possible pathogenesis of malformations of the urinary system in chromosomal disorders is discussed.

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References

  • Ashley, D. J., Mostofi, F. K.: Renal agenesis and dysgenesis. J. Urol. (Baltimore) 83, 211–230 (1960)

    Google Scholar 

  • Baxter, T. J.: Polycystic kidney of infants and children. Morphology, distribution and relation of the cysts. Nephron 2, 15–31 (1965)

    Google Scholar 

  • Beaudoing, A., Bost, M., Rambaud, P., Pasquier, B., Dumontel, C.: Renalni polycystoza u novorozence. Klinickopatologicke pozorovani. Mosaikova trisomie C. Čs. Pediat. 27, 223–224 (1972)

    Google Scholar 

  • Berghe, H. van den, Eygen, M. van, Fryns, J., Tanghe, W., Verresen, H.: Partial trisomy 1, karyotype 46, XY,12-,t (1q,12p) +. Hum. Genet. 18, 225–230 (1973)

    Google Scholar 

  • Bernstein, J.: Developmental abnormalities of the renal parenchyma-renal hypoplasia and dyplasia. Pathol. annual (New York) 3, 213–247 (1968)

    Google Scholar 

  • Blanck, C., Jalling, B., Lindsten, J., Zetterquist, P.: Trisomy 13–15. Report of a case with clinical, cytogenetic and pathologic findings. Acta path, microbiol. scand. 60, 36–46 (1964)

    Google Scholar 

  • Bocquet, L.: Pathologie comparée des trisomies D et E. Un. méd. Can. 97, 907–923 (1968)

    Google Scholar 

  • Butler, L. J., France, N. E., Jacoby, N. M.: An infant with multiple congenital anomalies and a ring chromosome in group C (X-6-12). J. med. Genet. 4, 295–298 (1967)

    Google Scholar 

  • Butler, L. J., Snodgrass, G., France, N., Sinclair, L., Russell, A.: E (16–18) trisomy syndrome: analysis of 13 cases. Arch. Dis. Childh. 40, 600–611 (1965)

    Google Scholar 

  • Cagianut, B., Theiler, K.: Bilateral colobomas of iris and chorioid, association with partial deletion of a chromosome of group D. Arch. Opthal. 83, 141–144 (1970)

    Google Scholar 

  • Egli, F., Stalder, G.: Malformations of kidney and urinary tract in common chromosomal aberrations. I. Clinical studies. Hum. Genet. 18, 1–15 (1973)

    Google Scholar 

  • Eys, J. van, Nance, W. E., Engel, E.: C-autosomal trisomy with mosaieism: a new syndrome ? Pediatrics 45, 665–671 (1970)

    Google Scholar 

  • Ferrandez, A., Schmid, W.: Potter-Syndrom (Nierenagenesie) mit chromosomaler Aberration beim Patient und Mosaik beim Vater. Helv. paediat. Acta 26, 210–214 (1971)

    Google Scholar 

  • Francke, U.: Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations. Amer. J. hum. Genet. 24, 189–213 (1972)

    Google Scholar 

  • Giorgi, P. L., Clecarelli, M., Paci, A.: Su un caso de sindrome del “cri du chat” con peculiari anomalie fenotipiche. Minerva pediat. 17, 1972–1975 (1965)

    Google Scholar 

  • Giovannucci, M., Calabri, G., Paoli, A.: La trisomia “D”. Su due casi con fenotipo caratteristico. Rivista Clin, pediat. 20, 1–10 (1969)

    Google Scholar 

  • Hirschhorn, K., Lucas, M., Wallace, I.: Precise identification of various chromosomal abnormalities. Ann. hum. Genet. 36, 375–379 (1973)

    Google Scholar 

  • Hole, H.: Chromosomenbefunde bei einem Foetus mit Zystenniere. Med. Welt 34, 1967–1968 (1967)

    Google Scholar 

  • Hoo, J. J., Obermann, U., Cramer, H.: The behaviour of ring chromosome 13. Hum. Genet. 24, 161–171 (1974)

    Google Scholar 

  • Hsu, L., Barcinski, M., Shapiro, L., Valderrama, E., Gertner, M., Hirschhorn, K.: Parental chromosomal aberrations associated with multiple abortions and an abnormal infant. Obstet, and Gynec. 36, 723–730 (1970)

    Google Scholar 

  • Huttová, M., Rusnák, M., Izakovič, V., Šuliková, Z.: Patauov syndróm-trizómia 13. Čs. Pediat. 26, 433–436 (1971)

    Google Scholar 

  • Jacobsen, P., Mikkelsen, M., Rosleff, F.: The trisomy 8 syndrome: report of two further cases. Ann. Génét. 17, 87–94 (1974)

    Google Scholar 

  • Juberg, R. C., Gilbert, E. F., Salisbury, R. S.: Trisomy C in an infant with polycystic kidneys and other malformations. J. Pediat. 76, 598–603 (1970)

    Google Scholar 

  • Kissane, J. M.: Congenital malformations. In: Pathology of the kidney, p. 63–117. London: Churchill 1966

    Google Scholar 

  • Kravtzova, G., Lazjuk, G.: Dysplasia of the kidneys. Archiv Patologii (Moscow) 37, N 2 3–12 (1975)

    Google Scholar 

  • Law, E. M., Masterson, J. G.: Familial 18q- syndrome. Ann. Génét. 12, 215–222 (1969)

    Google Scholar 

  • Lazjuk, G.: The principles of diagnostic of chromosomal disorders in the newborns. Materials of Xth Ail-Union Meeting of Pediaters. Moscow, 1974, 329–332

  • Lazjuk, G. I., Lurie, I. W., Kravtzova, G. I., Usoev, S. S.: New cytogenetic variant of Orbeli's syndrome (46.XY/45.XY.-D/46.XY.Dq+). Hum. Genet. 20, 219–221 (1973)

    Google Scholar 

  • Lazjuk, G., Kravtzova, G., Kulazhenko, V., Usova, Y., Usoev, S.: Analysis of 137 cases of trisomy D. Genetika (Moscow) 7, N 10, 116–129 (1971)

    Google Scholar 

  • Leisti, J.: Structural variation in human mitotic chromosomes. Ann. Acad. Sci. fenn. A 179, 1–62 (1971)

    Google Scholar 

  • Lejeune, J., Lafourcade, J., Grouchy, J. de, Berger, R., Gautier, M., Turpin, R.: Délétion partielle du bras court du chromosome 5. Individualisation d'un nouvel état morbide. Sem. Hôp. Paris 40, 1069–1079 (1964)

    Google Scholar 

  • Macintyre, M. N., Hempel, J. M., Staples, W. I., Stenchever, M. A.: A ring chromosome in a human male with congential anomalies. Anat. Rec. 148, 386 (1964)

    Google Scholar 

  • Malpuech, G., Dutrillaux, B., Fonck, Y., Gaulme, J., Bouche, B.: Trisomie 8 en mosaique. Arch, franç Pédiat. 29, 853–859 (1972)

    Google Scholar 

  • Masterson, J. G., Law, E. M., Rashad, M. N., Cahalane, S. F., Kavanagh, T. M.: A malformation syndrome with ring D chromosome. J. Irish med. Ass. 61, 398–399 (1968)

    Google Scholar 

  • Mikelsaar, A.-V. N., Lazjuk, G. L., Lurie, I. W., Tüür, S., Käosaar, M., Mikelsaar, R., Loolaid, V.: A 4p- syndrome. A case report. Hum. Genet. 19, 345–347 (1973)

    Google Scholar 

  • Mottet, N., Jensen, H.: The anomalous embryonic development associated with trisomy 13–15. Amer. J. clin. Path., 43, 334–347 (1965)

    Google Scholar 

  • O'Rahilly, R., Muecke, E. C.: The timing and sequence of events in the development of the human urinary system during the embryonic period proper. Z. Anat. Entwickl.-Gesch. 138, 99–109 (1972)

    Google Scholar 

  • Osathanondh, V., Potter, E.: Pathogenesis of polycystic kidneys. Type 4 due to urethral obstruction. Arch. Path. 77, 502–509 (1964)

    Google Scholar 

  • Papiernik-Berkhauer, E.: Enfant triploide à terme et thérapeutique hormonale. Bull. Féd. Soc. Gynéc. Obstét. franç. 20, 248–250 (1968)

    Google Scholar 

  • Passarge, E., Sutherland, J. M.: Potter's syndrome. Chromosome analysis of three cases with Potter's syndrome or related syndromes. Amer. J. Dis. Child. 109, 80–84 (1965)

    Google Scholar 

  • Pfeiffer, R. A.: Karyotyp und Phänotyp der autosomalen Chromosomenaberrationen beim Menschen. Stuttgart: Fischer 1968

    Google Scholar 

  • Picciano, D. J., Berlin, C. M., Davenport, S. L. H., Jacobson, C. B.: Human ring chromosomes: a report of five cases. Ann. Genet. 15, 241–247 (1972)

    Google Scholar 

  • Prats, J., Moragas, A.: Structural chromosome anomaly in a case of multiple malformations. Helv. paediat. Acta 22, 565–571 (1967)

    Google Scholar 

  • Pytel, A. J.: Handbook of clinical urology (Rus.). Moscow 1 (1969)

  • Reinwein, H., Schröter, R., Wegner, G., Wolf, U.: Chromosomenmosaik mit zwei aneuploide Stammlinien in der Gewebekultur bei einem Patienten mit multiplen Missbildungen. Helv. paediat. Aeta 21, 72–84 (1966)

    Google Scholar 

  • Saint-Rome, G., Gagnon, J., Jeliu, G., Duhaime, M.: La trisomie C libre homogène et en mosaique. Un. méd. Can. 101, 2121–2129 (1972)

    Google Scholar 

  • Schaohcnmann, G., Schmid, W., Fraccaro, M., Mannini, A., Tiepolo, L., Perona, G. P., Sartori, E.: Chromosomes in coloboma and anal atresia. Lancet 1965 II, 290

    Google Scholar 

  • Schepens, G., Glorieux, F., Buyl, M. L., Dourov, N., Koulisoher, L.: La trisomie 18. Etude de deux cas. Acta paediat. belg. 21, 71–90 (1967)

    Google Scholar 

  • Schinzel, A., Schmid, W.: Trisomie 18. Helv. paediat. Acta 26, 673–685 (1971)

    Google Scholar 

  • Schlegel, R. J., Aspillaga, M. J., Neu, R. L., Leao, J. C., Gardner, L. I.: XX chromosomes and renal agenesis. Lancet 1966 I, 819

    Google Scholar 

  • Schmickel, R. D., Silverman, E. M., Floyd, A. D., Payne, F. E., Pooley, J. M., Beck, M. L.: A live-bom infant with 69 chromosomes. J. Pediat. 79, 97–103 (1971)

    Google Scholar 

  • Shaw, M., Cohen, M. M., Hildebrandt, H.: A familial 4–5 reciprocal translocation resulting in partial trisomy B. Amer. J. hum. Genet. 17, 54–70 (1965)

    Google Scholar 

  • Stoll, C., Sacrez, R., Willard, D., Freysz, H.: Un cas de trisomie 18 avec aplasie bilatérale du radius et thrombopénie. Pédiatrie 27, 537–542 (1972)

    Google Scholar 

  • Surana, R. B., Conen, P. E.: Partial trisomy 4 resulting from a 4/18 reciprocal translocation. Ann. Genet. 15, 191–194 (1972)

    Google Scholar 

  • Taylor, A.: Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome. J. med. Genet. 5, 227–252 (1968)

    Google Scholar 

  • Taylor, A. I., Challacombe, D. N., Howlett, R. M.: Short-arm deletion, chromosome 4, (4p-), a syndrome? Ann. hum. Genet. 34, 137–144 (1970)

    Google Scholar 

  • Terplan, K., Lopez, E., Robinson, H.: Histological structural anomalies in the brain in trisomy 18 syndrome. Amer. J. Dis. Child. 119, 228–235 (1970)

    Google Scholar 

  • Tondury, G.: Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies. Hum. Genet. 18, 16–32 (1973)

    Google Scholar 

  • Witkowski, R.: A case of r(4). Personal communication (1972)

  • Yunis, J. J., Sanchez, O.: A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10. J. Pediat. 84, 567–570 (1974)

    Google Scholar 

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Kravtzova, G.I., Lazjuk, G.I. & Lurie, I.W. The malformations of the urinary system in autosomal disorders. Virchows Arch. A Path. Anat. and Histol. 368, 167–178 (1975). https://doi.org/10.1007/BF00432416

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