Asplenia in two father-son pairs

N. M. Lindor, W. A. Smithson, C. A. Ahumada, V. V. Michels, J. M. Opitz

Research output: Contribution to journalArticle

18 Scopus citations

Abstract

We report on two father-son pairs with isolated nonsyndromal asplenia. This may represent autosomal dominant inheritance of a mutation in a gene involved with spleen development and determination of laterality. The incidence of hereditary isolated asplenia is unknown; therefore, screening for asplenia in first degree relatives of individuals with (poly)asplenia should be considered.

Original languageEnglish (US)
Pages (from-to)10-11
Number of pages2
JournalAmerican journal of medical genetics
Volume56
Issue number1
DOIs
StatePublished - Mar 13 1995

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Lindor, N. M., Smithson, W. A., Ahumada, C. A., Michels, V. V., & Opitz, J. M. (1995). Asplenia in two father-son pairs. American journal of medical genetics, 56(1), 10-11. https://doi.org/10.1002/ajmg.1320560104