Literature DB >> 2405671

Chromosome 6q deletions: a report of two additional cases and a review of the literature.

D R McLeod1, S B Fowlow, A Robertson, D Samcoe, I Burgess, J J Hoo.   

Abstract

Here we report on two additional cases of distal 6q deletions with one case showing a terminal deletion of chromosome 6 (46,XY, del(6)(pter----q26:)) and one case showing an interstitial deletion of chromosome 6 (46,XY, del(6)(pter----q23::q25----qter)). The association of retinal abnormalities in 6q deletions is supported, and the additional manifestations of skin hyperextensibility, sacral abnormality, and imperforate anus are described.

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Year:  1990        PMID: 2405671     DOI: 10.1002/ajmg.1320350115

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


  7 in total

1.  Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss.

Authors:  Sandesh Chakravarthy Sreenath Nagamani; Ayelet Erez; Christine Eng; Zhishuo Ou; Craig Chinault; Laura Workman; James Coldwell; Pawel Stankiewicz; Ankita Patel; James R Lupski; Sau Wai Cheung
Journal:  Eur J Hum Genet       Date:  2008-11-26       Impact factor: 4.246

2.  Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.

Authors:  D Wieczorek; H Engels; R Viersbach; B Henke; G Schwanitz; E Passarge
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

3.  Necrotizing Enterocolitis in Two Siblings and an Unrelated Infant with Overlapping Chromosome 6q25 Deletions.

Authors:  Hannah C D Esdal; Muhammad B Ghbeis; Daniel A Saltzman; Donavon Hess; Janet R Hume; Robyn C Reed; Susan A Berry; Eric Hoggard; Betsy Hirsch; Linda B Baughn; Lisa A Schimmenti
Journal:  Mol Syndromol       Date:  2018-04-28

4.  Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech.

Authors:  Beate Peter; Hope Lancaster; Caitlin Vose; Kyle Middleton; Carol Stoel-Gammon
Journal:  Clin Linguist Phon       Date:  2017-09-21       Impact factor: 1.346

5.  Cytogenomic delineation and clinical follow-up of two siblings with an 8.5 Mb 6q24.2-q25.2 deletion inherited from a paternal insertion.

Authors:  Vera Ayres Meloni; Roberta Santos Guilherme; Mariana Moyses Oliveira; Michele Migliavacca; Sylvia Satomi Takeno; Nara Lygia Macena Sobreira; Maria de Fatima Faria Soares; Claudia Berlim de Mello; Maria Isabel Melaragno
Journal:  Am J Med Genet A       Date:  2014-06-04       Impact factor: 2.802

6.  Interstitial deletions at 6q14.1q15 associated with developmental delay and a marfanoid phenotype.

Authors:  R B Lowry; J E Chernos; M S Connelly; J P H Wyse
Journal:  Mol Syndromol       Date:  2013-08-01

Review 7.  A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature review.

Authors:  Stefano Stagi; Elisabetta Lapi; Marilena Pantaleo; Massimo Carella; Antonio Petracca; Agostina De Crescenzo; Leopoldo Zelante; Andrea Riccio; Maurizio de Martino
Journal:  BMC Med Genet       Date:  2015-08-23       Impact factor: 2.103

  7 in total

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