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Diaphragmatic hernia in a female newborn with focal dermal hypoplasia and marked asymmetric malformations (Goltz-Gorlin Syndrome)

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Abstract

We report a female newborn with focal dermal hypoplasia (Goltz-Gorlin Syndrome) and marked asymmetric malformations on the right side of the body. Diaphragmatic hernia on the same side, which has not been reported in this syndrome, led to perinatal complications.

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References

  1. Barta, L., Lengyel, J.: Über ein Syndrom mit naeviformen Hautatrophien (systematisierte naeviforme Atrophodermie). Ann. Paediatr., (Basel) 207, 4, 258–268 (1966)

    Google Scholar 

  2. Beganovic, N., Lommen, E. J. P.: A case of focal dermal hypoplasia (Goltz syndrome) with some new aspects. Acta Paediatr. Scand. 66, 255–256 (1977)

    Google Scholar 

  3. Cole, H. H., Driver, J. R., Giffen, H. K., Norris, C. B., Stroud, B.: Ectodermal and mesodermal dysplasia with osseous involvement. Arch. Derm. Syph. (Paris) 44, 773–787 (1941)

    Google Scholar 

  4. Daly, J. F.: Focal dermal hypoplasia. Cutis 4, 1354–1359 (1968)

    Google Scholar 

  5. Ferrara, A.: Goltz's syndrome. Am. J. Dis. Child. 123, 263 (1972)

    Google Scholar 

  6. Goltz, R. W., Peterson, C. W., Gorlin, R. J., Ravits, G. H.: Focal dermal hypoplasia. Arch. Derm. 86, 708–717 (1962)

    Google Scholar 

  7. Goltz, R. W., Henderson, R. R., Hitch, J. M., Ott, J. E.: Focal dermal hypoplasia syndrome. Review of the literature and report of two cases. Arch. Derm. 101, 1–11 (1970)

    Google Scholar 

  8. Gorlin, R. J., Meskin, L. H., Peterson, W. C., Jr., Goltz, R. W.: Focal dermal hypoplasia syndrome. Acta derm.-venereol. (Stockh.) 43, 421–440 (1963)

    Google Scholar 

  9. Hailey, H., Hailey, H., Clemens, H.: Poikiloderma congenitale. Arch. Derm. Syph. 44, 345–348 (1941)

    Google Scholar 

  10. Hernandez-Perez, E., Diag-Perallon, J. R.: Enfermedad de Liebermann-Cole (hipoplasia dermica focal). Med. Cutanea 3, 393–398 (1969)

    Google Scholar 

  11. Holden, J. D., Akers, W. A.: Goltz's syndrome: focal dermal hypoplasia. Amer. J. Dis. Child. 114, 292–300 (1967)

    Google Scholar 

  12. Howell, J. B.: Nevus angiolipomatosus vs focal dermal hypoplasia. Arch. Derm. 92, 238–248 (1965)

    Google Scholar 

  13. Jessner, M.: Verhandlungen der Breslauer dermatologischen Vereinigung. Arch. Derm. Syph. (Berl.) 133, 48 (1921)

    Google Scholar 

  14. Jessner, M.: Naeviforme, poikilodermie-artige Hautveränderungen mit Mißbildungen (Schwimmhautbildung an den Fingern, Papillome am Anus). Zentralbl. Haut- u. Geschlkr. 27, 46 (1928)

    Google Scholar 

  15. Kunze, J., Frenzel, U. H., Hüttig, E., Grosse, R.-R., Wiedemann, H.-R.: Klinefelter's syndrome and incontinentia pigmenti Bloch-Sulzberger. Hum. Genet. 35, 237–240 (1977)

    Google Scholar 

  16. Lanzieri, M.: Su di una rara associazione di sindrome malformativa cranio-facciale e di assenza congenita del perone. Ann. Ottalmol. Clin. Ocul. 87, 667–678 (1961)

    Google Scholar 

  17. Leisti, J., Hallman, M.: Focal dermal hypoplasia with marked asymmetry. Birth Defects: Original Article Series, Vol XIII, No. 3C. The National Foundation 1977, March of Dimes, A. R. Liss. Inc., New York

  18. Lenz, W.: Medizinische Genetik, p. 95. Stuttgart: Thieme 1979

    Google Scholar 

  19. Liebermann, S. L.: Atrophodermia linearis maculosa et papillomatosus congenitalis. Acta Derm. Venereol. (Stockh.) 16, 476–484 (1935)

    Google Scholar 

  20. Martin-Scott, I.: Congenital focal dermal hypoplasia. Brit. J. Derm. 77, 60–62 (1965)

    Google Scholar 

  21. Miedzinski, F.: Naevus lipomatodes superficialis. Dermatologica. 126, 223–228 (1963)

    Google Scholar 

  22. Ruiz-Maldonado, R., Carnevale, A., Tamayo, L., Milonas de Montiel, E.: Focal dermal hypoplasia. Clin. Genet. 6, 36–45 (1974)

    Google Scholar 

  23. Smith, D. W.: Recognizable patterns of human malformations. 2nd edition, pp. 320–321. Philadelphia, London, Toronto: W. B. Saunders Company 1976

    Google Scholar 

  24. Stollmann, K.: Bisher noch nicht beschriebene Befunde bei Incontinentia pigmenti. Derm. Wschr. 153, 489–496 (1967)

    Google Scholar 

  25. Temtamy, S., McKusick, V.: The gentics of hand malformations. Birth Defects: Original Article Series, Vol. XIV, No. 3, p. 526 (1978)

    Google Scholar 

  26. Toro-Sola, M. A., Kistenmacher, M. L., Punnett, H. H., Digeorge, A. M.: Focal dermal hypoplasia syndrome in a male. Clin. Genet. 7, 325–327 (1975)

    Google Scholar 

  27. Valerius, N. H.: A case of focal dermal hypoplasia syndrome (Goltz) with bilateral cheilognatho-palatoschisis. Acta Paediatr. Scand. 63, 287–288 (1974)

    Google Scholar 

  28. Walbaum, R., Samaille, G., Dehaene, P.: Syndrome de Goltz chez un garçon. Pédiatrie 25, 911–920 (1970)

    Google Scholar 

  29. Wodniansky, P.: Über die Formen der congenitalen Poikilodermie. Arch. Klin. Exp. Dermatol. 205, 331–342 (1957)

    Google Scholar 

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Authors and Affiliations

  1. Department of Pediatrics, University of Kiel, Schwanenweg 20, D-2300, Kiel, Federal Republic of Germany

    J. Kunze, K. Heyne & H.-R. Wiedemann

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  1. J. Kunze
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  2. K. Heyne
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  3. H.-R. Wiedemann
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Kunze, J., Heyne, K. & Wiedemann, HR. Diaphragmatic hernia in a female newborn with focal dermal hypoplasia and marked asymmetric malformations (Goltz-Gorlin Syndrome). Eur J Pediatr 131, 213–218 (1979). https://doi.org/10.1007/BF00538945

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  • DOI: https://doi.org/10.1007/BF00538945

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