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. 1968 Feb;43(227):73–79. doi: 10.1136/adc.43.227.73

Angiokeratoma corporis diffusum. Some clinical aspects.

A W Johnston, S D Weller, B J Warland
PMCID: PMC2019899  PMID: 5642987

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Selected References

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

  1. BROWN A., MILNE J. A. Diffuse angiokeratoma: report of two cases with diffuse skin changes, one with neurological symptoms and splenomegaly. Glasgow Med J. 1952 Sep;33(9):361–367. [PMC free article] [PubMed] [Google Scholar]
  2. CURRY H. B., FLEISHER T. L. Angiokeratoma corporis diffusum--a case report. JAMA. 1961 Mar 11;175:864–868. doi: 10.1001/jama.1961.03040100028008. [DOI] [PubMed] [Google Scholar]
  3. DUPERRAT B. [Fabry's diffuse angiokeratoma (angiokeratoma corporis diffusum)]. Presse Med. 1959 Oct 24;67:1814–1816. [PubMed] [Google Scholar]
  4. FONE D. J., KING W. E. ANGIOKERATOMA CORPORIS DIFFUSUM (FABRY'S SYNDROME). Australas Ann Med. 1964 Nov;13:339–348. doi: 10.1111/imj.1964.13.4.339. [DOI] [PubMed] [Google Scholar]
  5. Frost P., Tamala Y., Spaeth G. L. Fabry's disease--glycolipid lipidosis. Histochemical and electron microscopic studies of two cases. Am J Med. 1966 Apr;40(4):618–627. doi: 10.1016/0002-9343(66)90123-9. [DOI] [PubMed] [Google Scholar]
  6. HASHIMOTO K., GROSS B. G., LEVER W. F. ANGIOKERATOMA CORPORIS DIFFUSUM (FABRY). HISTOCHEMICAL AND ELECTRON MICROSCOPIC STUDIES OF THE SKIN. J Invest Dermatol. 1965 Feb;44:119–128. [PubMed] [Google Scholar]
  7. Johnston A. W., Warland B. J., Weeller S. D. Genetic aspects of angiokeratoma corporis diffusum. Ann Hum Genet. 1966 Jul;30(1):25–41. doi: 10.1111/j.1469-1809.1966.tb00004.x. [DOI] [PubMed] [Google Scholar]
  8. Jorgensen M. B., Jorgensen B. B. Angiokeratoma corporis diffusum (Fabry). An account of two cases--one with central nervous involvement. Dan Med Bull. 1965 Oct;12(6):152–157. [PubMed] [Google Scholar]
  9. Opitz J. M., Stiles F. C., Wise D., Race R. R., Sanger R., Von Gemmingen G. R., Kierland R. R., Cross E. G., De Groot W. P. The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus. Am J Hum Genet. 1965 Jul;17(4):325–342. [PMC free article] [PubMed] [Google Scholar]
  10. PRICE J. H. Angiokeratoma corporis diffusum. Br J Dermatol. 1955 Mar;67(3):105–109. doi: 10.1111/j.1365-2133.1955.tb12700.x. [DOI] [PubMed] [Google Scholar]
  11. RAHMAN A. N. The ocular manifestations of hereditary dystopic lipidosis (angiokeratoma corporis diffusum universale). Arch Ophthalmol. 1963 Jun;69:708–716. doi: 10.1001/archopht.1963.00960040714005. [DOI] [PubMed] [Google Scholar]
  12. SWEELEY C. C., KLIONSKY B. FABRY'S DISEASE: CLASSIFICATION AS A SPHINGOLIPIDOSIS AND PARTIAL CHARACTERIZATION OF A NOVEL GLYCOLIPID. J Biol Chem. 1963 Sep;238:3148–3150. [PubMed] [Google Scholar]
  13. WISE D., WALLACE H. J., JELLINEK E. H. Angiokeratoma corporis diffusum. A clinical study of eight affected families. Q J Med. 1962 Apr;31:177–206. [PubMed] [Google Scholar]
  14. WYERS J. G., BRUGGE R. J., POMPE C. A., PIJPERS P. M. HISTOLOGISCHE ASPECTEN BIJ DE ZIEKTE VAN FABRY (ANGIOKERATOMA CORPORIS DIFFUSUM) Ned Tijdschr Geneeskd. 1965 Mar 20;109:548–560. [PubMed] [Google Scholar]

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