--- abstract: 'We have reported a case of Yunis-Varon syndrome which is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones, characteristic facial features, abnormalities of the fingers and/or toes & cleidocranial dysplasia. Additional features in this case were patent ductus arteriosus, CT brain findings suggestive of ischemic changes, CSF examination suggestive of pyogenic meningitis & cystic changes in right adrenal gland.' altloc: - http://www.ojhas.org/issue34/2010-2-16.htm chapter: ~ commentary: ~ commref: ~ confdates: ~ conference: ~ confloc: ~ contact_email: ~ creators_id: - dal.sameer@gmail.com - ~ creators_name: - family: Dal given: SI honourific: '' lineage: '' - family: Parmar given: P honourific: '' lineage: '' date: 2010-07-30 date_type: published datestamp: 2010-09-13 03:51:06 department: ~ dir: disk0/00/00/70/15 edit_lock_since: ~ edit_lock_until: 0 edit_lock_user: ~ editors_id: - Kakkilaya BS editors_name: - family: Kakkilaya given: Srinivas honourific: Dr lineage: '' eprint_status: archive eprintid: 7015 fileinfo: /style/images/fileicons/application_pdf.png;/7015/1/2010%2D2%2D16.pdf full_text_status: public importid: ~ institution: ~ isbn: ~ ispublished: pub issn: ~ item_issues_comment: [] item_issues_count: 0 item_issues_description: [] item_issues_id: [] item_issues_reported_by: [] item_issues_resolved_by: [] item_issues_status: [] item_issues_timestamp: [] item_issues_type: [] keywords: 'Yunis-Varon syndrome, distal aphalangea' lastmod: 2011-03-11 08:57:44 latitude: ~ longitude: ~ metadata_visibility: show note: ~ number: 2 pagerange: ~ pubdom: TRUE publication: Online Journal of Health and Allied Sciences publisher: Dr. B.S. Kakkilaya refereed: TRUE referencetext: "1.\tYunis E, Varon H. Cleidocranial dysostosis, severe micrognathism, bilateral absence of thumbs and first metatarsal bone, and distal aphalangea: A new genetic syndrome. Am J Dis Child 1980;134:649-653,\r\n2.\tHuges HE, Partington MW. Brief clinical report: the syndrome of Yunis and Varon - report of a further case. Am J Med Genet 1983;14:539-544 \r\n3.\tPfeiffer RA, Diekmann L, Stock HJ. Aplasia of the thumbs and great toes as the outstanding feature of Yunis and Varon syndrome: A new entity, a new observation. Ann Genet 1988;31:241-243.\r\n4.\tJones KL. Smith’s Recognizable Patterns of Human Malformation. 5th edition. Philadelphia. WB Saunders Company.1997. pp 410-411.\r\n5.\tAdes LC, Morris LL, Richardson M, Pearson C, Haan EA. Congenital heart malformation in Yunis-Varon syndrome. J Med Genet 1993;30:788-792.\r\n6.\tPartington ME. Cardiomyopathy added to the Yunis Varon syndrome. Proc Greenwood Genet 1988;7:224-225 \r\n7.\tWalch E, Schmidt M, Brenner RE, Emons D, Dame C, Pontz B, et al. Yunis-Varon syndrome: Evidence for a lysosomal storage disease. Am J Med Genet 2000;95:157-160. \r\n8.\tDworzak F, Mora M, Borroni C, Cornelio F, Blasevich F, Cappellini A, et al. Generalized lysosomal storage in Yunis-Varon syndrome. Neuromuscul Disord 1995;5:423-428. \r\n9.\tBhatia S, Holla RG. Yunis Varon syndrome. Indian Pediatr 2005;42:373-375.\r\n10.\tKulkarni ML, Vani HN, Nagendra K et al. Yunis Varon Syndrome. Indian J Pediatr 2006;73(4):353-355." relation_type: [] relation_uri: [] reportno: ~ rev_number: 19 series: ~ source: ~ status_changed: 2010-09-13 03:51:06 subjects: - OJHAS succeeds: ~ suggestions: ~ sword_depositor: ~ sword_slug: ~ thesistype: ~ title: Yunis Varon Syndrome type: journale userid: 4338 volume: 9