Co-existence of Two Rare Conditions: Oculo-Palato-Cerebral Syndrome and Congenital Chylothorax
محل انتشار: مجله علمی ناباروری ایران، دوره: 9، شماره: 3
سال انتشار: 1397
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 380
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شناسه ملی سند علمی:
JR_IRJN-9-3_013
تاریخ نمایه سازی: 12 تیر 1398
چکیده مقاله:
Background: Oculo-palato-cerebral syndrome is an extremely rare condition characterized by various features, including low-birth weight, microcephaly, cerebral atrophy, mild-to-severe developmental delay, cleft palate, persistent hyperplastic primary vitreous, microphthalmia, small hands and feet, joint laxity, and large ears with thick helices. Diagnosis of this syndrome is based on the clinical manifestations, particularly the presence of persistent hyperplastic primary vitreous in association with other malformations. Congenital chylothorax is also a rare condition in the neonatal period, which is caused by the abnormal accumulation of the lymphatic fluid within the pleural space. This condition may be detected prenatally or during the neonatal period. Case report: We presented the case of a patient with oculo-palato-cerebral syndrome and congenital chylothorax based on a literature review. Conclusion: Oculo-palato-cerebral syndrome and congenital chylothorax are both rare conditions. To the best of our knowledge, this was the first case report on congenital chylothorax in association with oculo-palato-cerebral syndrome in the available literature. Since there have only been five case reports on these patients, further evidence is required to confirm the possible association between these rare conditions.
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نویسندگان
Seyhan Erisir Oygucu
Division of Neonatology, Department of Pediatrics, Faculty of Medicine, University of Kyrenia, Sehit Yahya Bakır Sokak, Karakum, Kyrenia, North Cyprus
Gonul Tezel
Division of Neonatology, Department of Pediatrics, Antalya Training and Research Hospital, Antalya, Turkey
Muhammet Kazim Erol
.Department of Ophthalmology, Antalya Training and Research Hospital, Antalya, Turkey
Ozgur Erkal
Division of Medical Genetics, Department of Pediatrics, Antalya Training and Research Hospital, Antalya, Turkey