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Iranian Journal of Neonatology، جلد ۹، شماره ۳، صفحات ۸۳-۸۷
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Co-existence of Two Rare Conditions: Oculo-Palato-Cerebral Syndrome and Congenital Chylothorax |
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| چکیده انگلیسی 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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| کلیدواژه‌های انگلیسی مقاله |
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| نویسندگان مقاله |
| 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
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| نشانی اینترنتی |
http://ijn.mums.ac.ir/article_11529.html |
| فایل مقاله |
اشکال در دسترسی به فایل - ./files/site1/rds_journals/231/article-231-868088.pdf |
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| زبان مقاله منتشر شده |
en |
| موضوعات مقاله منتشر شده |
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