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Severe combined immunodeficiency disease

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Severe combined immunodeficiency disease is a heterogenous group of autosomal or X linked recessive disorders characterised by markedly decreased T and B cell function. Defects in the normal ossification of foetal cartilage (dysostosis) and adenosine deaminase deficiency are common.

The overall incidence of SCID is 2 per million, but the rate is higher in some groups, for example, Apache Indians.


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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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