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Osteogenesis Imperfecta and Constipation: A Case Report
Osteogenesis imperfecta (OI) is a heterogeneous group of heritable group of disorders in which the amount of type-1 collagen is decreased or the type 1 collagen is abnormal . 90% of cases are due to autosomal dominant mutations, while the remaining 10% are due to autosomal recessive mutations or of unknown cause. Type III was found to be associated... Read More»
Case Report: J Gastrointest Dig Syst 2011,S3:003
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