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POSTER PRESENTATION Open Access Alendronate treatment for osteogenesis imperfecta type III in twin babies: a case report Annang Giri Moelyo * , Septin Widiretnani, Ani Suryandari From 7th APPES Biennial Scientific Meeting Nusa Dua, Bali. 14-17 November 2012 Osteogenesis Imperfecta (OI) is a connective tissue disorders. There are several types of OI. OI can be autoso- mal dominant, some cases can be found in recessive by mosaicism in the parent. The main goal of treatment is to reduce the incidence of fractures, prevent deformities of bones and scoliosis, and improve the functional patient. This is a case of OI given alendronate as an alternative treatment. Twin boys babies born in Moewardi Hospital by sectio caesaria. Baby I and II seemed swollen on both of hand and leg. Both of the babies appeared to be less active and limitation of range of motion, with blue sclera. Result of x- rays, it appeared multiple fractures in extremities and costae. We diagnosed osteogenesis omperfecta type III, clinically. We gave alendronate 1 x 1 mg orally, because sodium pamidronate was not available at that time. Alendronate were given by thirty to forty five degree posi- tion. Orthopedic surgeon gave on conservative therapy by slap. During treatment in hospital, appeared new fractures in each baby. After giving alendronate therapy for 4 months, the baby I didnt show new fractures, the baby II suffered three new fractures. There were no side effect of alendronate treatment on gastrointestinal. At the aged of 5th month, the patients were given intravenously sodium pamidronate for 3 days with a dose of 2 mg. Three months after pamidronate, the baby I didnt show new fractures, the baby II suffered one new fracture. Bone mineral density was not performed in these patients. We conclude that oral biphosphonate could be alternative treatment for OI if intravenous biphosphonate is unavailable. It still needs more reseach regarding to effectiveness of oral biphosphonate compare to intravenous biphosphonate. Published: 3 October 2013 doi:10.1186/1687-9856-2013-S1-P158 Cite this article as: Moelyo et al.: Alendronate treatment for osteogenesis imperfecta type III in twin babies: a case report. International Journal of Pediatric Endocrinology 2013 2013(Suppl 1):P158. Submit your next manuscript to BioMed Central and take full advantage of: Convenient online submission Thorough peer review No space constraints or color figure charges Immediate publication on acceptance Inclusion in PubMed, CAS, Scopus and Google Scholar Research which is freely available for redistribution Submit your manuscript at www.biomedcentral.com/submit Child Health Department, Faculty of Medicine Sebelas Maret University Moewardi Hospital, Surakarta, Indonesia Moelyo et al. International Journal of Pediatric Endocrinology 2013, 2013(Suppl 1):P158 http://www.ijpeonline.com/content/2013/S1/P158 © 2013 Moelyo et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Alendronate treatment for osteogenesis imperfecta type III in twin babies: a case report

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POSTER PRESENTATION Open Access

Alendronate treatment for osteogenesisimperfecta type III in twin babies: a case reportAnnang Giri Moelyo*, Septin Widiretnani, Ani Suryandari

From 7th APPES Biennial Scientific MeetingNusa Dua, Bali. 14-17 November 2012

Osteogenesis Imperfecta (OI) is a connective tissuedisorders. There are several types of OI. OI can be autoso-mal dominant, some cases can be found in recessive bymosaicism in the parent. The main goal of treatment is toreduce the incidence of fractures, prevent deformities ofbones and scoliosis, and improve the functional patient.This is a case of OI given alendronate as an alternativetreatment.Twin boys babies born in Moewardi Hospital by sectio

caesaria. Baby I and II seemed swollen on both of handand leg. Both of the babies appeared to be less active andlimitation of range of motion, with blue sclera. Result of x-rays, it appeared multiple fractures in extremities andcostae. We diagnosed osteogenesis omperfecta type III,clinically. We gave alendronate 1 x 1 mg orally, becausesodium pamidronate was not available at that time.Alendronate were given by thirty to forty five degree posi-tion. Orthopedic surgeon gave on conservative therapy byslap. During treatment in hospital, appeared new fracturesin each baby. After giving alendronate therapy for 4months, the baby I didn’t show new fractures, the baby IIsuffered three new fractures. There were no side effect ofalendronate treatment on gastrointestinal. At the aged of5th month, the patients were given intravenously sodiumpamidronate for 3 days with a dose of 2 mg. Three monthsafter pamidronate, the baby I didn’t show new fractures,the baby II suffered one new fracture. Bone mineraldensity was not performed in these patients. We concludethat oral biphosphonate could be alternative treatment forOI if intravenous biphosphonate is unavailable. It stillneeds more reseach regarding to effectiveness of oralbiphosphonate compare to intravenous biphosphonate.

Published: 3 October 2013

doi:10.1186/1687-9856-2013-S1-P158Cite this article as: Moelyo et al.: Alendronate treatment forosteogenesis imperfecta type III in twin babies: a case report.International Journal of Pediatric Endocrinology 2013 2013(Suppl 1):P158.

Submit your next manuscript to BioMed Centraland take full advantage of:

• Convenient online submission

• Thorough peer review

• No space constraints or color figure charges

• Immediate publication on acceptance

• Inclusion in PubMed, CAS, Scopus and Google Scholar

• Research which is freely available for redistribution

Submit your manuscript at www.biomedcentral.com/submitChild Health Department, Faculty of Medicine Sebelas Maret University

Moewardi Hospital, Surakarta, Indonesia

Moelyo et al. International Journal of Pediatric Endocrinology 2013, 2013(Suppl 1):P158http://www.ijpeonline.com/content/2013/S1/P158

© 2013 Moelyo et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative CommonsAttribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction inany medium, provided the original work is properly cited.