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Osteogenesis imperfecta type V: A repost of two Filipino families and review of literature
Acta Medica Philippina ; : 74-79, 2015.
Article in En | WPRIM | ID: wpr-632830
Responsible library: WPRO
ABSTRACT
Osteogenesis imperfecta (Ol) type V is distinct Ol phenotype that has recently been described. Patients with this phenotype present characteristically with interosseous membrane calcification and hyperplastic callus formation. We present the clinical and radiographic characteristics of two Filipino families diagnosed to have Ol type V. Through this review of cases, we aim to educate healthcare providers by highlighting salient clinical and radiographic features to aid in the recognition of this specific Ol phenotype, difficulties in diagnosis, current practices in management and fracture prevention, and issues in genetic counseling.
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Full text: 1 Database: WPRIM Main subject: Osteogenesis Imperfecta / Patients / Phenotype / Bony Callus / Diagnosis / Genetic Counseling Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Acta Medica Philippina Year: 2015 Document type: Article
Full text: 1 Database: WPRIM Main subject: Osteogenesis Imperfecta / Patients / Phenotype / Bony Callus / Diagnosis / Genetic Counseling Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Acta Medica Philippina Year: 2015 Document type: Article
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