Osteogenesis imperfecta: a case report

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dc.contributor.authorT., Kambiakdiken_US
dc.contributor.authorSohi, Inderpreeten_US
dc.contributor.authorNyorak, Tolien_US
dc.contributor.authorKumar, Pawam Kumaren_US
dc.contributor.authorSangma, Sengseng R.en_US
dc.contributor.authorZosanglianien_US
dc.date.accessioned2020-09-24T07:45:08Z
dc.date.available2020-09-24T07:45:08Z
dc.date.issued2019-09
dc.description.abstractOsteogenesis imperfecta (OI) is a group of rare inherited disorders of connective tissue with the common feature of excessive fragility of bones caused by mutations in collagen. Diagnosis is mainly based on the clinical features of the disorder. We report a late preterm a male neonate born to a 20 years old primigravida. He had clinical features of a type II OI and severe birth asphyxia.en_US
dc.identifier.affiliationsDepartment of Paediatrics, Regional Institute of Medical Sciences, Imphal, Manipur, Indiaen_US
dc.identifier.affiliationsDepartment of Paediatrics, Christian Medical College and Hospital, Ludhiana, Panjab, Indiaen_US
dc.identifier.citationT. Kambiakdik, Sohi Inderpreet, Nyorak Toli, Kumar Pawam Kumar, Sangma Sengseng R., Zosangliani. Osteogenesis imperfecta: a case report. International Journal of Contemporary Pediatrics. 2019 Sep; 6(5): 2219-2221en_US
dc.identifier.issn2349-3283
dc.identifier.issn2349-3291
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/204271
dc.languageenen_US
dc.publisherMedip Academyen_US
dc.relation.issuenumber5en_US
dc.relation.volume6en_US
dc.source.urihttps://dx.doi.org/10.18203/2349-3291.ijcp20193756en_US
dc.subjectAlkaline phosphataseen_US
dc.subjectBluish scleraen_US
dc.subjectFragile bonesen_US
dc.subjectOsteogenesis Imperfectaen_US
dc.subjectWormian bonesen_US
dc.titleOsteogenesis imperfecta: a case reporten_US
dc.typeJournal Articleen_US
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