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. 1991 Aug;28(8):541–543. doi: 10.1136/jmg.28.8.541

Pallister-Killian syndrome: additional manifestations of cleft palate and sacral appendage.

D R McLeod 1, L R Wesselman 1, D I Hoar 1
PMCID: PMC1016985  PMID: 1920372

Abstract

We report a case of Pallister-Killian syndrome in a 28 week gestation infant. In addition to the characteristic phenotype, this patient had a cleft palate, diaphragmatic hernia, sacral appendage, and imperforate anus. The lymphocyte karyotype showed 96% 46,XX/4% 47,XX+i (12p) and the fibroblast karyotype 47,XX,+marker (presumed i(12p]. Fibroblast cytogenetic studies should be considered in all cases of diaphragmatic hernia associated with other malformations.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Buyse M. L., Korf B. R. "Killian Syndrome", Pallister mosaic syndrome, or mosaic tetrasomy 12P? - an analysis. J Clin Dysmorphol. 1983 Fall;1(3):2–5. [PubMed] [Google Scholar]
  2. Hunter A. G., Clifford B., Cox D. M. The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome. Clin Genet. 1985 Jul;28(1):47–53. doi: 10.1111/j.1399-0004.1985.tb01217.x. [DOI] [PubMed] [Google Scholar]
  3. Killian W., Zonana J., Schroer R. J. Abnormal hair, craniofacial dysmorphism, and severe mental retardation - a new syndrome? J Clin Dysmorphol. 1983 Fall;1(3):6–13. [PubMed] [Google Scholar]
  4. Lopes V., Mak E., Wyatt P. R. Prenatal diagnosis of tetrasomy 21. Prenat Diagn. 1985 May-Jun;5(3):233–235. doi: 10.1002/pd.1970050312. [DOI] [PubMed] [Google Scholar]
  5. Moerman P., Fryns J. P., Vandenberghe K., Devlieger H., Lauweryns J. M. The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome. Am J Med Genet. 1988 Dec;31(4):805–814. doi: 10.1002/ajmg.1320310413. [DOI] [PubMed] [Google Scholar]
  6. Pauli R. M., Zeier R. A., Sekhon G. S. Mosaic isochromosome 12p. Am J Med Genet. 1987 Jun;27(2):291–294. doi: 10.1002/ajmg.1320270207. [DOI] [PubMed] [Google Scholar]
  7. Reynolds J. F., Daniel A., Kelly T. E., Gollin S. M., Stephan M. J., Carey J., Adkins W. N., Webb M. J., Char F., Jimenez J. F. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases. Am J Med Genet. 1987 Jun;27(2):257–274. doi: 10.1002/ajmg.1320270204. [DOI] [PubMed] [Google Scholar]
  8. Warburton D., Anyane-Yeboa K., Francke U. Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases. Am J Med Genet. 1987 Jun;27(2):275–283. doi: 10.1002/ajmg.1320270205. [DOI] [PubMed] [Google Scholar]
  9. Wyatt P. R. Pallister-Killian syndrome--an update of a clinical case. Am J Med Genet. 1988 Jan;29(1):229–229. doi: 10.1002/ajmg.1320290133. [DOI] [PubMed] [Google Scholar]

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