Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/1249
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dc.contributor.authorPriti SL, Mulimani MS Nivedita K-
dc.date.accessioned2019-11-16T12:11:27Z-
dc.date.available2019-11-16T12:11:27Z-
dc.date.issued2015-
dc.identifier.issn22316809-
dc.identifier.urihttp://hdl.handle.net/123456789/1249-
dc.description.abstractA 20 year old male patient presented with ascites since birth, swelling of right scrotum, absence of development of secondary sexual characters, breathlessness on exertion, short limb gait, and hematemesis. Ultrasound imaging and CT angiography of the abdomen revealed absence of portal vein, thrombus at the junction of superior mesenteric vein and splenic vein, cavernous transformation and development of collaterals. Echocardiography revealed hypertrophic obstructive cardiomyopathy (HOCM) and X-ray hip revealed absence of head of femur. Scrotal examination revealed right sided indirect inguinal hernia and hydrocoele. A diagnosis of Goldenhar syndrome was madeen_US
dc.language.isoenen_US
dc.publisherBLDE(Deemed to be University)en_US
dc.subjectGoldenhar Syndrome, Hematemesis, Hypertrophic Cardiomyopathy, Inguinal Hernia, Scrotumen_US
dc.titleGoldenhar Syndrome.en_US
dc.typeArticleen_US
Appears in Collections:Faculty of General Medicine

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