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. 1977 Apr;14(2):91–99. doi: 10.1136/jmg.14.2.91

Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles.

M W Spence, A L Goldbloom, J K Burgess, D D'entremont, B A Ripley, K L Weldon
PMCID: PMC1013521  PMID: 404411

Abstract

Heterozygote detection for angiokeratoma corporis diffusum (Anderson-Fabry disease, ACD), an X-linked disorder of glycosphingolipid metabolism was examined using alpha-galactosidase activity, an alpha-galactosidase/beta-galactosidase activity ratios (alpha/beta ratio) in leucocytes, plasma, and hair follicles; For leucocytes, 22 obligate heterozygotes, 25 suspected heterozygotes, and 47 control subjects were studied, while for plasma, the groups were 17 obligate heterozygotes and 35 controls. The alpha/beta ratio in plasma and leucocytes was clearly a better discriminator between obligate heterozygotes and controls than alpha-galactosidase activity alone, but still failed to detect 3 obligates with leucocytes and 2 with plasma. Discrimination was not improved by joint use of plasma and leucocyte alpha/beta ratios, but was improved by measurement of hair-follicle alpha/beta ratios. The interdecile range of log (alpha-galactosidase/beta-galactosidase activity) in 20 hair follicles from each of 4 obligate and 7 suspected heterozygotes was clearly different from 11 control subjects. Accordingly, for rapid screening for carriers of ACD, we recommend use of leucocyte or plasma alpha/beta ratios which should detect greater than 85% of heterozygotes. When results are equivocal, and ancillary information suggests heterozygous status, the more time-consuming measurement of hair-follicle alpha/beta ratios is a useful additional test.

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Selected References

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

  1. Avila J. L., Convit J., Velazquez-Avila G. Fabry's disease: normal alpha-galactosidase activity and urinary-sediment glycosphingolipid levels in two obligate heterozygotes. Br J Dermatol. 1973 Aug;89(2):149–157. doi: 10.1111/j.1365-2133.1973.tb02951.x. [DOI] [PubMed] [Google Scholar]
  2. Beutler E., Kuhl W. Biochemical and electrophoretic studies of -galactosidase in normal man, in patients with Fabry's disease, and in Equidae. Am J Hum Genet. 1972 May;24(3):237–249. [PMC free article] [PubMed] [Google Scholar]
  3. Brady R. O., Gal A. E., Bradley R. M., Martensson E., Warshaw A. L., Laster L. Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency. N Engl J Med. 1967 May 25;276(21):1163–1167. doi: 10.1056/NEJM196705252762101. [DOI] [PubMed] [Google Scholar]
  4. DAVIDSON R. G., NITOWSKY H. M., CHILDS B. DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS. Proc Natl Acad Sci U S A. 1963 Sep;50:481–485. doi: 10.1073/pnas.50.3.481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Danes B. S., Bearn A. G. Hurler's syndrome: a genetic study of clones in cell culture with particular reference to the Lyon hypothesis. J Exp Med. 1967 Sep 1;126(3):509–522. doi: 10.1084/jem.126.3.509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Del Monte M. A., Johnson D. L., Cotlier E., Krivit W., Desnick R. J. Letter: Diagnosis of Fabry's disease by tear alpha-galactosidase A. N Engl J Med. 1974 Jan 3;290(1):57–58. doi: 10.1056/NEJM197401032900118. [DOI] [PubMed] [Google Scholar]
  7. Desnick R. J., Allen K. Y., Desnick S. J., Raman M. K., Bernlohr R. W., Krivit W. Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes. J Lab Clin Med. 1973 Feb;81(2):157–171. [PubMed] [Google Scholar]
  8. Francke U., Bakay B., Nyhan W. L. Detection of heterozygous carriers of the Lesch-Nyhan syndrome by electrophoresis of hair root lysates. J Pediatr. 1973 Mar;82(3):472–478. doi: 10.1016/s0022-3476(73)80123-4. [DOI] [PubMed] [Google Scholar]
  9. Gartler S. M., Gandini E., Angioni G., Argiolas N. Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells. Ann Hum Genet. 1969 Oct;33(2):171–176. doi: 10.1111/j.1469-1809.1969.tb01642.x. [DOI] [PubMed] [Google Scholar]
  10. Gartler S. M., Gansini E., Hutchison H. T., Campbell B., Zechhi G. Glucose-6-phosphate dehydrogenase mosaicism: ito;ozatopm om tje study of hair follicle variegation. Ann Hum Genet. 1971 Jul;35(1):1–7. [PubMed] [Google Scholar]
  11. Gartler S. M., Scott R. C., Goldstein J. L., Campbell B. Lesch-Nyhan syndrome: rapid detection of heterozygotes by use of hair follicles. Science. 1971 May 7;172(3983):572–574. doi: 10.1126/science.172.3983.572. [DOI] [PubMed] [Google Scholar]
  12. Ho M. W., Beutler S., Tennant L., O'Brien J. S. Fabry's disease: evidence for a physically altered -galactosidase. Am J Hum Genet. 1972 May;24(3):256–266. [PMC free article] [PubMed] [Google Scholar]
  13. Kattamis C. A. Glucose-6-phosphate dehydrogenase deficiency in female heterozygotes and the X-inactivation hypothesis. Acta Paediatr Scand. 1967;(Suppl):103+–103+. doi: 10.1111/j.1651-2227.1967.tb15284.x. [DOI] [PubMed] [Google Scholar]
  14. Kint J. A. Fabry's disease: alpha-galactosidase deficiency. Science. 1970 Feb 27;167(3922):1268–1269. doi: 10.1126/science.167.3922.1268. [DOI] [PubMed] [Google Scholar]
  15. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  16. LYON M. F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. doi: 10.1038/190372a0. [DOI] [PubMed] [Google Scholar]
  17. Mapes C. A., Anderson R. L., Sweeley C. C. Galactosylgalactosylglucosylceramide: Galactosyl hydrolase in normal human plasma and its absence in patients with fabry's disease. FEBS Lett. 1970 Apr 2;7(2):180–182. doi: 10.1016/0014-5793(70)80151-x. [DOI] [PubMed] [Google Scholar]
  18. Mapes C. A., Sweeley C. C. Galactosyl (alpha 1--4)galactosylceramide: galactosyl hydrolase activity in normal and Fabry plasma. Biochem Biophys Res Commun. 1973 Aug 21;53(4):1317–1324. doi: 10.1016/0006-291x(73)90609-8. [DOI] [PubMed] [Google Scholar]
  19. Mapes C. A., Sweeley C. C. Preparation and properties of an affinity column adsorbent for differentiation of multiple forms of -galactosidase activity. J Biol Chem. 1973 Apr 10;248(7):2461–2470. [PubMed] [Google Scholar]
  20. Mapes C. A., Sweeley C. C. Substrate specificity of ceramide trihexosidase. FEBS Lett. 1972 Sep 15;25(2):279–281. doi: 10.1016/0014-5793(72)80503-9. [DOI] [PubMed] [Google Scholar]
  21. McKnight M. T., Spence M. W. Attempted detection of heterozygotes for maple-syrup-urine disease. Clin Genet. 1972;3(6):458–464. doi: 10.1111/j.1399-0004.1972.tb01481.x. [DOI] [PubMed] [Google Scholar]
  22. Migeon B. R., Der Kaloustian V. M., Nyhan W. L., Yough W. J., Childs B. X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations. Science. 1968 Apr 26;160(3826):425–427. doi: 10.1126/science.160.3826.425. [DOI] [PubMed] [Google Scholar]
  23. O'Brien J. S., Okada S., Chen A., Fillerup D. L. Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay. N Engl J Med. 1970 Jul 2;283(1):15–20. doi: 10.1056/NEJM197007022830104. [DOI] [PubMed] [Google Scholar]
  24. Philippart M., Sarlieve L., Manacorda A. Urinary glycolipids in Fabry's disease. Their examination in the detection of atypical variants and the pre-symptomatic state. Pediatrics. 1969 Feb;43(2):201–206. [PubMed] [Google Scholar]
  25. Rietra P. J., Tager J. M., de Groot W. P. Detection of Fabry hemizygotes and heterozygotes by measurement of -galactosidase in urine. Clin Chim Acta. 1972 Aug;40(1):229–235. doi: 10.1016/0009-8981(72)90275-6. [DOI] [PubMed] [Google Scholar]
  26. Romeo G., Migeon B. R. Genetic inactivation of the alpha-galactosidase locus in carriers of Fabry's disease. Science. 1970 Oct 9;170(3954):180–181. doi: 10.1126/science.170.3954.180. [DOI] [PubMed] [Google Scholar]
  27. Silvers D. N., Cox R. P., Balis M. E., Dancis J. Detection of heterozygote in Lesch-Nyhan disease by hair-root analysis. N Engl J Med. 1972 Feb 24;286(8):390–395. doi: 10.1056/NEJM197202242860802. [DOI] [PubMed] [Google Scholar]
  28. Spence M. W., Ripley B. A., Embil J. A., Tibbles J. A. A new variant of Sandhoff's disease. Pediatr Res. 1974 Jun;8(6):628–637. doi: 10.1203/00006450-197406000-00003. [DOI] [PubMed] [Google Scholar]
  29. Stamatoyannopoulos G., Papayannopoulou T., Bakopoulos C., Motulsky A. G. Detection of glucose-6-phosphate dehydrogenase deficient heterozygotes. Blood. 1967 Jan;29(1):87–101. [PubMed] [Google Scholar]
  30. Wood S., Nadler H. L. Fabry's disease: absence of an -galactosidase isozyme. Am J Hum Genet. 1972 May;24(3):250–255. [PMC free article] [PubMed] [Google Scholar]

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