Literature DB >> 7573135

Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.

D M White1, D A Pillers, J A Reiss, M G Brown, R E Magenis.   

Abstract

Interstitial deletions of chromosome 4 have been described rarely and have had variable presentations. We describe the phenotypic characteristics associated with interstitial deletion of the p14-16 region of chromosome 4 in 7 patients with multiple minor anomalies in common, and with mental retardation. A review of published cases of interstitial deletions of the short arm of chromosome 4 is provided. These deletions present a distinct phenotype which is different from that of Wolf-Hirschhorn syndrome.

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Year:  1995        PMID: 7573135     DOI: 10.1002/ajmg.1320570415

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism.

Authors:  Dong Li; Alanna Strong; Cuiping Hou; Helen Downes; Amanda Barone Pritchard; Pamela Mazzeo; Elaine H Zackai; Laura K Conlin; Hakon Hakonarson
Journal:  Mol Cytogenet       Date:  2022-08-05       Impact factor: 1.904

2.  LETM1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this condition.

Authors:  Lesley Hart; Anita Rauch; Antony M Carr; Joris R Vermeesch; Mark O'Driscoll
Journal:  Dis Model Mech       Date:  2014-03-13       Impact factor: 5.758

  2 in total

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