Neonatal Osteogenesis Imperfecta : A Case Report

Irman Permana*, Tatan Tandu Bela*, Ineu Nopita*, Arum Ardisa

Rini*, Evania Risya*, Rahmat Ibnu Hasan*

Department of Child Health, Faculty of Medicine Universitas Swadaya Gunung

Jati*, Waled District Hospital, Cirebon*

Introduction: Osteogenesis Imperfecta (OI) is

Case Report:

Discussion:

Conclusion: We conclude from our study that most common in female baby,
keywords: Neonatal Osteogenesis Imperfecta, pregnancy, congenital

Introduction

Osteogenesis imperfecta (OI) is a genetic disorder characterized by bones

that break easily, often from little or no apparent cause.

Case Report

We present the case of female baby 3 days was born by 25 years old
primipara mother at serotinous term by normal vaginal delivery in Waled
Hospital. Mother do not have congenital abnormalities and their family too. Baby
do not cry immediately after birth and had no dermatological lesions. Her birth
weight was 2540 gram, length 40 cm and head circumference 29 cm, all of them
is below the normal range standard for a newborn.
The baby at birth did not immediately cry and baby’s skin looked blue
with amniotic meconial and apgar score 5/6. Then treated by sucking mucus in the
nose and mouth of the baby then dry the baby's body and keep warm and set the
position. After that, the baby is given oxygen and stimulate the baby to cry. The
body temperature was measured as 36,9°C, a heart rate of 140 beats per minute
and respiratory rate of 42 per minute.

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Discussion

Conclusion

We conclude from our study that most common in female baby,

commonly noticed in the primigravida.

Reference