Literature DB >> 8652084

A Croatian case of the Schinzel-Giedion syndrome.

V Culić1, B Resic, J W Oorthuys, W C Overweg-Plandsoen, R C Hennekam.   

Abstract

The Schinzel-Giedion syndrome is an infrequently described malformation syndrome, mainly characterized by a profound mental deficiency, a typical face including a midface hypoplasia, urogenital abnormalities, and minor radiographic features. Death prior to two year of age is the rule. A boy with typical features of the syndrome is described. He died at the age of 21 months. This is the first case of this syndrome reported from Croatia. The recurrence in only one of the 20 families, does not firmly sustain an autosomal recessive pattern of inheritance, although this still remains possible.

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Year:  1996        PMID: 8652084

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  3 in total

Review 1.  Schinzel-Giedion syndrome: a novel case, review and revised diagnostic criteria.

Authors:  Wei-Liang Liu; Zhi-Xu He; Fang Li; Rong Ai; Hong-Wei Ma
Journal:  J Genet       Date:  2018-03       Impact factor: 1.166

2.  Scoliosis in a case of Schinzel-Giedion syndrome.

Authors:  Amit K Sharma; Joseph A Gonzales
Journal:  HSS J       Date:  2009-06-17

3.  Clinical and radiological findings in Schinzel-Giedion syndrome.

Authors:  Mudaffer Al-Mudaffer; Christine Oley; Sue Price; Ian Hayes; Alison Stewart; Christine M Hall; William Reardon
Journal:  Eur J Pediatr       Date:  2008-05-07       Impact factor: 3.183

  3 in total

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