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Cytomegalic inclusion disease (medical condition): A cytomegalus virus infection that occurs before birth.
See also:
Wyatt disease:
»Introduction: Wyatt disease
»Symptoms of Wyatt disease
Cytomegalic inclusion disease: caused by cytomegalovirus, a member of the Herpesviridae family; the presence of inclusion bodies within the cytoplasm and nuclei of enlarged cells of various organs of newborn infants dying with jaundice, hepatomegaly, splenomegaly, purpura, thrombocytopenia, and fever; the condition also occurs, at all ages, as a complication of other diseases in which immune mechanisms are severely depressed, and has been found incidentally in salivary gland epithelium, apparently as a localized or mild infection (salivary gland virus disease). SYN: cytomegalovirus disease, inclusion body disease.
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.
These medical condition or symptom topics may be relevant to medical information for Cytomegalic inclusion disease:
Cytomegalic inclusion disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Cytomegalic inclusion disease, or a subtype of Cytomegalic inclusion disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Cytomegalic inclusion disease: Another name for Wyatt disease (or close medical condition association).
»Introduction: Wyatt disease
»Symptoms of Wyatt disease
Some of the symptoms of Cytomegalic inclusion disease incude:
See full list of 14 symptoms of Cytomegalic inclusion disease (Wyatt disease)
Source - NIH
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