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Fibrochondrogenesis
- ... COL11A1 gene have been identified in people with fibrochondrogenesis type 1, a disorder of bone growth characterized ... abnormalities, hearing loss, and vision loss. Infants with fibrochondrogenesis type 1 have a very narrow chest that ...
- ... COL11A2 gene have been identified in people with fibrochondrogenesis type 2, a disorder of bone growth characterized ... severe skeletal abnormalities and hearing loss. Infants with fibrochondrogenesis type 2 have a very narrow chest that ...