Goldenhar Syndrome.

Priti SL, Mulimani MS Nivedita K

dc.contributor.author	Priti SL, Mulimani MS Nivedita K
dc.date.accessioned	2019-11-16T12:11:27Z
dc.date.available	2019-11-16T12:11:27Z
dc.date.issued	2015
dc.identifier.issn	22316809
dc.identifier.uri	http://hdl.handle.net/123456789/1249
dc.description.abstract	A 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 made	en_US
dc.language.iso	en	en_US
dc.publisher	BLDE(Deemed to be University)	en_US
dc.subject	Goldenhar Syndrome, Hematemesis, Hypertrophic Cardiomyopathy, Inguinal Hernia, Scrotum	en_US
dc.title	Goldenhar Syndrome.	en_US
dc.type	Article	en_US