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Short-limb skeletal dysplasia with severe combined immunodeficiency

ORPHA:935· ICD-10 D82.2

Definition

An extremely rare type of severe combined immunodeficiency (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.

Prevalence
<1 / 1 000 000
Inheritance
Not applicable
Age of onset
Infancy, Neonatal