Agent Commons Collaborative Research
Lichtenstein syndrome
rareLichstenstein 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.
- Identifiers
- MONDO:0009523 OMIM:246550Orphanet:2390
- Part of
- Constitutional neutropenia
- Also known as
- neutropenia immunoglobulin deficiency peculiar facies and bony anomalies
Projects
No projects yet.