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. 1977 Jun;14(3):172–176. doi: 10.1136/jmg.14.3.172

Genetic study of Welsh gypsies.

E M Williams, P R Harper
PMCID: PMC1013551  PMID: 881706

Abstract

A South Wales gypsy kindred of Romany origin had a high incidence of phenylketonuria along with other recessively inherited disorders. There was a high degree of consanguinity (F = 0-017) with an excess of non-specific mental subnormality among known consanguineous matings. Phenylketonuria and a number of other recessively inherited disorders have been recorded from other Romany gypsy populations, but it is uncertain whether this results from a generally high gene frequency for the disorders or from consanguinity and other more local factors.

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Selected References

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

  1. Avcin M. Gypsy isolates in Slovenia. J Biosoc Sci. 1969 Jul;1(3):221–233. [PubMed] [Google Scholar]
  2. BLEHOVA J., DANESOVA J., GREC L., HAJEK F., MATOUSEK M., VOJTIK V. Vyskyt fenylketonurie Cechách a na Moravé. Cesk Pediatr. 1959 Jun 5;14(6):498–503. [PubMed] [Google Scholar]
  3. Bradley D. M. Screening for inherited metabolic disease in Wales using urine-impregnated filter paper. Arch Dis Child. 1975 Apr;50(4):264–268. doi: 10.1136/adc.50.4.264. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CARTER C. O., WOOLF L. I. The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England. Ann Hum Genet. 1961 May;25:57–64. doi: 10.1111/j.1469-1809.1961.tb01497.x. [DOI] [PubMed] [Google Scholar]
  5. HUTCHISON J. H., MCGIRR E. M. Sporadic non-endemic goitrous cretinism; hereditary transmission. Lancet. 1956 Jun 30;270(6931):1035–1037. doi: 10.1016/s0140-6736(56)90800-5. [DOI] [PubMed] [Google Scholar]
  6. Harper P. S. Genetic variation in Wales. J R Coll Physicians Lond. 1976 Jul;10(4):321–332. [PMC free article] [PubMed] [Google Scholar]
  7. Harper P. S., Williams E. M. Letter: Genetic disorders in gypsies. Lancet. 1975 May 3;1(7914):1041–1041. doi: 10.1016/s0140-6736(75)91995-9. [DOI] [PubMed] [Google Scholar]
  8. Passarge E. Letter: Genetic disorders in gypsies. Lancet. 1975 May 31;1(7918):1243–1243. doi: 10.1016/s0140-6736(75)92232-1. [DOI] [PubMed] [Google Scholar]
  9. Saugstad L. F. Anthropological significance of phenylketonuria. Clin Genet. 1975 Jan;7(1):52–61. [PubMed] [Google Scholar]
  10. Thalhammer O., Gitzelmann R., Pantlitschko M. Hypergalactosemia and galactosuria due to galactokinase deficiency in a newborn. Pediatrics. 1968 Sep;42(3):441–445. [PubMed] [Google Scholar]
  11. Van de Kamp J. J., Oving H., Giesbets M. A. Een patiënt met kinky hair disease (zierte van Menkers) Ned Tijdschr Geneeskd. 1975 Mar 29;119(13):505–510. [PubMed] [Google Scholar]

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