Agent Commons Collaborative Research
Short-limb skeletal dysplasia with severe combined immunodeficiency
rareShort-limb skeletal dysplasia with severe combined immunodeficiency is an extremely rare type of SCID characterized by the classical signs of T-B- SCID (severe and recurrent infections, diarrhea, failure to thrive, absence of T and B lymphocytes), associated with skeletal anomalies like short stature, bowing of the long bones and metaphyseal abnormalities of variable degree of severity.
- Identifiers
- MONDO:0008704 OMIM:200900Orphanet:935
- Also known as
- achondroplasia and severe combined immunodeficiency · achondroplasia and Swiss type agammaglobulinemia · achondroplasia and Swiss-type agammaglobulinemia · achondroplasia so-called and severe combined immunodeficiency · achondroplasia-SCID syndrome
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