Association of Goldenhar with Duane’s Retraction Syndrome
نویسندگان
چکیده
منابع مشابه
Goldenhar syndrome with contralateral pulmonary aplasia: a rare association.
We present a case of a 13-year-old boy with clinical features of Goldenhar syndrome (hemifacial microsomia with malformed ears) and associated contralateral pulmonary aplasia. The patient did not have any associated respiratory symptoms. Pulmonary aplasia is an uncommon association of Goldenhar Syndrome. A case of contralateral pulmonary aplasia has been rarely reported in the literature to the...
متن کاملCraniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract
Craniofacial microsomia (CFM) includes a spectrum of malformations primarily involving structures derived from the first and second branchial arches. Patients with hemifacial microsomia and epibulbar dermoids are said to have Goldenhar syndrome (GHS). Four-month-old boy with whitish pupillary reflex presented with the features of GHS in pediatric ophthalmology clinic. The child had ocular and a...
متن کاملGoldenhar Syndrome with Unusual Features
*Senior Resident, **Associate Professor, ***Professor, Department of Ophthalmology, T.N.M.C. and B.Y.L. Nair Hospital, Mumbai. Abstract Goldenhar syndrome is a morphogenetic anomaly involving the 1st and 2nd branchial arches. It is also known as the oculo-auriculo-vertebral syndrome because of the association of eye anomalies with or without vertebral and ear anomalies. It has been also Goldenh...
متن کامل[Goldenhar syndrome].
We present a report on 9 patients with Goldenhar's Syndrome, and the criteria used for the diagnosis. Familiar data and clinical characteristics. Are described and discussed with that of other authors. The medical literature about this syndrome shows a lack of uniformity on the criteria necessary to diagnose the syndrome, as well as the role of the pathogenic factors. The authors propose the ad...
متن کاملGoldenhar Syndrome
Goldenhar syndrome (Oculo-Auriculo-Vertebral Spectrum) (OAVS) is a rare congenital condition characterized by craniofacial abnormalities associated with anomalies of the spine, heart, kidney, central nervous and gastrointestinal system. Craniofacial abnormalities include the incomplete development of the eye, ear, nose, soft palate, lips and jaw. We report a case of Goldenhar syndrome in a 14-y...
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ژورنال
عنوان ژورنال: Delhi Journal of Ophthalmology
سال: 2020
ISSN: 0972-0200,2454-2784
DOI: 10.7869/djo.606