Literature DB >> 7277427

Ring chromosome 14: a distinct clinical entity.

R Schmidt, L Eviatar, H M Nitowsky, M Wong, S Miranda.   

Abstract

An infant girl with ring chromosome 14 is presented. The findings in this patient and in six previously reported cases of a ring 14 suggest that a characteristic clinical syndrome is associated with this chromosome aberration. The major features of the ring chromosome 14 syndrome include mental retardation, a disorder of skin pigmentation, seizures, and dysmorphic features, including flat occiput, epicanthal folds, downward slanting eyes, flat nasal bridge, upturned nostrils, short neck, and large low set ears.

Entities:  

Mesh:

Year:  1981        PMID: 7277427      PMCID: PMC1048739          DOI: 10.1136/jmg.18.4.304

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  6 in total

1.  Extended evaluation of previously reported twins with a ring 14 chromosome.

Authors:  R S Sparkes; I Klisak; M C Sparkes
Journal:  Ann Genet       Date:  1977-12

2.  [Ring chromosome 14 in monozygotic twins].

Authors:  P Jalbert; B Sele; H Jalbert; L Sirand; H Pison; J Couturier
Journal:  Ann Genet       Date:  1977-03

3.  [The Dr syndrome. Study of a further case (46, XX, 14r)].

Authors:  S Gilgenkrantz; C Cabrol; C Lausecker; M E Hartleyb; B Bohe
Journal:  Ann Genet       Date:  1971-03

4.  The 13q-deletion syndrome.

Authors:  P W Allderdice; J G Davis; O J Miller; H P Klinger; D Warburton; D A Miller; F H Allen; C A Abrams; E McGilvray
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

5.  Ring chromosomes in two infants with congenital malformations.

Authors:  M A Varela; W H Sternberg
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

6.  A ring 14 chromosome with deleted short arm.

Authors:  A P Amarose; E Dorus; P R Huttenlocher; S Csaszar
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  6 in total
  8 in total

Review 1.  Terminal deletion (14)(q32.3): a new case.

Authors:  N Telford; D A Thomson; M J Griffiths; S Ilett; J L Watt
Journal:  J Med Genet       Date:  1990-04       Impact factor: 6.318

2.  A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation.

Authors:  F S Yen; P E Podruch; B Weisskopf
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

Review 3.  Current status of human chromosome 14.

Authors:  D Kamnasaran; D W Cox
Journal:  J Med Genet       Date:  2002-02       Impact factor: 6.318

Review 4.  Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Authors:  I T Thomas; J L Frias; E S Cantu; C Z Lafer; D B Flannery; J G Graham
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

5.  De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

Authors:  D T Bonthron; S J Smith; J Fantes; C M Gosden
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

6.  Retinal/macular pigmentation in conjunction with ring 14 chromosome.

Authors:  P J Howard; D Clark; J Dearlove
Journal:  Hum Genet       Date:  1988-10       Impact factor: 4.132

7.  Distal monosomy 14 not associated with ring formation.

Authors:  S J Hreidarsson; J Stamberg
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

Review 8.  Guideline recommendations for diagnosis and clinical management of Ring14 syndrome-first report of an ad hoc task force.

Authors:  Berardo Rinaldi; Alessandro Vaisfeld; Sergio Amarri; Chiara Baldo; Giuseppe Gobbi; Pamela Magini; Erto Melli; Giovanni Neri; Francesca Novara; Tommaso Pippucci; Romana Rizzi; Annarosa Soresina; Laura Zampini; Orsetta Zuffardi; Marco Crimi
Journal:  Orphanet J Rare Dis       Date:  2017-04-11       Impact factor: 4.123

  8 in total

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