Literature DB >> 3881954

Deletions of the long arm of chromosome 6: two new cases and review of the literature.

R S Young, G S Fidone, P A Reider-Garcia, K L Hansen, J L McCombs, C M Moore.   

Abstract

Seven terminal deletions and four interstitial deletions of 6q have been reported. We present the clinical and cytogenetic findings of these cases and of two new patients with different interstitial deletions of 6q. Although there are too few cases of interstitial deletions to identify one or more clinical syndromes associated with monosomies of the more proximal regions of 6q, a terminal 6q deletion syndrome is proposed. Its major components are microcephaly with mental retardation, strabismus, apparently low-set malformed ears, a broad nasal bridge, micrognathia, apparently short neck, congenital heart defect, abnormal palmar creases, and various hand abnormalities.

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Year:  1985        PMID: 3881954     DOI: 10.1002/ajmg.1320200105

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


  8 in total

1.  Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalities.

Authors:  H R Slater; A Robb; L A Forsyth; D A Hamilton; M C Clark; C A Galloway
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

2.  Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.

Authors:  Jill A Rosenfeld; Dina Amrom; Eva Andermann; Frederick Andermann; Martin Veilleux; Cynthia Curry; Jamie Fisher; Stephen Deputy; Arthur S Aylsworth; Cynthia M Powell; Kandamurugu Manickam; Bryce Heese; Melissa Maisenbacher; Cathy Stevens; Jay W Ellison; Sheila Upton; John Moeschler; Wilfredo Torres-Martinez; Abby Stevens; Robert Marion; Elaine Maria Pereira; Melanie Babcock; Bernice Morrow; Trilochan Sahoo; Allen N Lamb; Blake C Ballif; Alex R Paciorkowski; Lisa G Shaffer
Journal:  Neurogenetics       Date:  2012-01-05       Impact factor: 2.660

3.  Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors:  J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

4.  Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.

Authors:  N Rubtsov; G Senger; H Kuzcera; A Neumann; C Kelbova; K Junker; V Beensen; U Claussen
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

5.  Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans.

Authors:  E Treacy; C Polychronakos; M Vekemans; P Eydoux; S Blaichman; H Scarpelli; M Ross; Y Xu; V M Der Kaloustian
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

6.  Ventricular septal defect with mobile tricuspid valve pouch mimicking tetralogy of Fallot.

Authors:  G L Johnson; W N O'Connor; S M Verble; C M Cottrill; J A Noonan
Journal:  Pediatr Cardiol       Date:  1986       Impact factor: 1.655

7.  Proximal Deletion of 6q Overlapping with Toriello-Carey Facial Phenotype: Prenatal Findings, Clinical Course, Differential Diagnosis, and Review.

Authors:  Sofía Catena; Mariana Aracena; Óscar Pizarro; Karena Espinoza; Guillermo Lay-Son
Journal:  Mol Syndromol       Date:  2017-11-29

8.  Rare presentation of 6q16.3 microdeletion syndrome with severe upper limb reduction defects and duodenal atresia.

Authors:  Megan L Donahue; Luis O Rohena
Journal:  Clin Case Rep       Date:  2017-04-26
  8 in total

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