Elhaddadi Hasnae, Ayyad Anass, Messaoudi Sahar, Amrani Rim
Department of Pediatrics, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Department of Neonatology and Neonatal Resuscitation, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Cureus. 2024 May 23;16(5):e60945. doi: 10.7759/cureus.60945. eCollection 2024 May.
Osteogenesis imperfecta (OI) is a rare inherited skeletal disease, characterized by bone fragility and low bone density. There are several types of OI, varying in severity from benign to severe. We report a case of type II OI, which is a lethal form according to the Sillence classification. At birth, the newborn presented immediate respiratory distress. Postnatal examination and bone radiography confirmed the diagnosis of OI type IIA. The genetic analysis was done along with genetic counseling. Death occurred on day nine of life due to respiratory failure secondary to pulmonary hypoplasia.
成骨不全症(OI)是一种罕见的遗传性骨骼疾病,其特征为骨骼脆弱和骨密度低。OI有几种类型,严重程度从良性到严重不等。我们报告一例II型OI病例,根据席尔尼斯分类,这是一种致死型。出生时,新生儿立即出现呼吸窘迫。产后检查和骨骼X线摄影确诊为IIA型OI。进行了基因分析并提供了遗传咨询。患儿于出生后第9天因肺发育不全继发呼吸衰竭死亡。