Lichtenstein syndrome
MONDO:0009523Lichstenstein syndrome is characterized by frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive.
Also known as: Lichtenstein syndrome, neutropenia immunoglobulin deficiency peculiar facies and bony anomalies
42 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials