Literature DB >> 1860515

Heart disease associated with deletion of the short arm of chromosome 18.

H R Movahhedian1, H A Kane, D Borgaonkar, M McDermott, S Septimus.   

Abstract

Deletion of the short arm of chromosome 18 provides a highly variable phenotype. Mental retardation, short stature, and abnormal facies are invariably present. About 9 percent of patients with this syndrome have cardiac pathology. An additional case with congenital heart disease has been presented along with a review of the literature concerning the association of congenital heart disease and the 18p- syndrome.

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Year:  1991        PMID: 1860515

Source DB:  PubMed          Journal:  Del Med J        ISSN: 0011-7781


  2 in total

Review 1.  Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.

Authors:  Beate Schmidt; Floris Udink ten Cate; Michael Weiss; Udo Koehler
Journal:  Eur J Pediatr       Date:  2012-07       Impact factor: 3.183

2.  Patent ductus arteriosus and pulmonary valve stenosis in a patient with 18p deletion syndrome.

Authors:  Chun-Hong Xie; Jian-Bin Yang; Fang-Qi Gong; Zheng-Yan Zhao
Journal:  Yonsei Med J       Date:  2008-06-30       Impact factor: 2.759

  2 in total

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