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Results 1 - 6 of 6 for Asplenia
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  1. Isolated congenital asplenia 
    Isolated congenital asplenia is a condition in which affected individuals are missing their spleen (asplenia) but have no other developmental abnormalities. While ...
    https://medlineplus.gov/.../condition/isolated-congenital-asplenia - Genetics
  2. Stormorken syndrome 
    ... Other features include lack of a functioning spleen (asplenia), scaly skin (ichthyosis), headaches, and difficulty with reading ... in their family. Stormorken-Sjaastad-Langslet syndrome Thrombocytopathy, asplenia, and miosis Genetic Testing Registry: Stormorken syndrome Stormorken- ...
    https://medlineplus.gov/genetics/condition/stormorken-syndrome - Genetics
  3. RPSA gene 
    ... have been identified in individuals with isolated congenital asplenia. People with this condition do not have a ... L, Casanova JL. Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated ...
    https://medlineplus.gov/genetics/gene/rpsa - Genetics
  4. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy 
    ... hypertension), or a small (atrophic) or absent spleen (asplenia). APECED occurs in about 1 in 90,000 ...
    https://medlineplus.gov/...inopathy-candidiasis-ectodermal-dystrophy - Genetics
  5. Primary ciliary dyskinesia 
    ... In addition, affected individuals may lack a spleen (asplenia) or have multiple spleens (polysplenia). Heterotaxy syndrome results ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
  6. Heterotaxy syndrome 
    ... can cause a person to have no spleen (asplenia) or multiple small, poorly functioning spleens (polysplenia). The ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics