A Case of Osteogenesis Imperfecta Congenita Diagnosed in Utero

スポンサーリンク

概要

• 論文の詳細を見る

• Osteogenesis imperfecta is a rare disorder characterized by abnormal fragility of the bones resulting in fractures after minimal trauma, blue sclerotics, and deafness because of osteosclerosis.Recently, we have experienced a case of osteogenesis imperfecta congenita diagnosed in utero.A 24 year-old woman, gravida 1, para 1, who complained of weak fetal movement. The presentation and position of the fetus in the uterus was obscure at 35 weeks. We took prenatal X-ray film and fetography. Prenatal X-ray film did not show the fetal bone clearly, and fetography showed that the extremities were short. Consequently, we diagnosed osteogenesis imperfecta congenita in utero.The external appearance of the newborn showed enlargement of the head, softness of the calvarium, deformity of the extremities, and blue sclera. The X-ray film of the newborn showed multiple fractures of the ribs extremities. According to the laboratory findings of the case, serum calcium and lymphatic cells were increased. Because ribs and vertebrae showed disturbance of ossification, histopathological diagnosis was osteogenesis imperfecta congenita.

• 近畿産科婦人科学会の論文

近畿産科婦人科学会 | 論文

• 当院における卵巣粘液性腺癌の治療経験の検討
• 婦人科癌末期の難治性イレウスに対する減圧目的の経皮的内視鏡的胃瘻造設について
• 子宮体癌の保存的治療後妊娠での前置癒着胎盤に対し内腸骨動脈バルーン留置下で帝王切開および子宮全摘術を施行した1例
• 当科の卵巣粘液性腺癌の治療成績 : ─リンパ節郭清の適応についての考察
• 妊娠糖尿病を合併した高度肥満妊婦の分娩誘発の1例

もっと見る

スポンサーリンク