دورية أكاديمية

Goldenhar Syndrome Associated with Extensive Arterial Malformations

التفاصيل البيبلوغرافية
العنوان: Goldenhar Syndrome Associated with Extensive Arterial Malformations
المؤلفون: Renee Frances Modica, L. Daphna Yasova Barbeau, Jennifer Co-Vu, Richard D. Beegle, Charles A. Williams
المصدر: Case Reports in Pediatrics, Vol 2015 (2015)
بيانات النشر: Hindawi Limited, 2015.
سنة النشر: 2015
المجموعة: LCC:Pediatrics
مصطلحات موضوعية: Pediatrics, RJ1-570
الوصف: Goldenhar Syndrome is characterized by craniofacial, ocular and vertebral defects secondary to abnormal development of the 1st and 2nd branchial arches and vertebrae. Other findings include cardiac and vascular abnormalities. Though these associations are known, the specific anomalies are not well defined. We present a 7-month-old infant with intermittent respiratory distress that did not improve with respiratory interventions. Echocardiogram suggested a double aortic arch. Cardiac CT angiogram confirmed a right arch and aberrant, stenotic left subclavian artery, dilation of the main pulmonary artery, and agenesis of the left thyroid lobe. Repeat echocardiograms were concerning for severely dilated coronary arteries. Given dilation, a rheumatologic workup ensued, only identifying few weakly positive autoantibodies. Further imaging demonstrated narrowing of the aorta below the renal arteries and extending into the common iliac arteries and proximal femoral arteries. Given a physical exam devoid of rheumatologic findings, only weakly positive autoantibodies, normal inflammatory markers, and presence of the coronary artery dilation, the peripheral artery narrowings were not thought to be vasculitic. This case illustrates the need to identify definitive anomalies related to Goldenhar Syndrome. Although this infant’s presentation is rare, recognition of specific vascular findings will help differentiate Goldenhar Syndrome from other disease processes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2090-6803
2090-6811
العلاقة: https://doaj.org/toc/2090-6803Test; https://doaj.org/toc/2090-6811Test
DOI: 10.1155/2015/954628
الوصول الحر: https://doaj.org/article/b5ccfceecb374d66bba6439d250ef21fTest
رقم الانضمام: edsdoj.b5ccfceecb374d66bba6439d250ef21f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20906803
20906811
DOI:10.1155/2015/954628