Literature DB >> 1711306

Miller-Dieker syndrome with ring chromosome 17.

N Sharief1, J Craze, D Summers, L Butler, C B Wood.   

Abstract

A girl presented at 6 weeks of age with failure to thrive and arching of the back. She had various dysmorphic features, hepatosplenomegaly, and developmental delay. The electroencephalogram and cranial ultrasound were abnormal, and a computed tomogram showed lissencephaly and apparent agenesis of the corpus callosum. Because of frequent aspiration she became oxygen dependent. She later developed intractable convulsions and died at the age of 9 months.

Entities:  

Mesh:

Year:  1991        PMID: 1711306      PMCID: PMC1793146          DOI: 10.1136/adc.66.6.710

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  15 in total

Review 1.  Ring chromosome 17 in a mentally retarded boy.

Authors:  O H Qazi; C Madahar; R Kanchanapoomi; R Giridharan; E Beller
Journal:  Ann Genet       Date:  1979

2.  Ring 17 chromosome detected by amniocentesis.

Authors:  A G Weinberg; J L Bair; M J Harrod
Journal:  Humangenetik       Date:  1975-07-23

3.  Miller-Dieker syndrome and monosomy 17p13: a new case.

Authors:  A Selypes; A László
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

4.  Miller-Dieker syndrome: lissencephaly and monosomy 17p.

Authors:  W B Dobyns; R F Stratton; J T Parke; F Greenberg; R L Nussbaum; D H Ledbetter
Journal:  J Pediatr       Date:  1983-04       Impact factor: 4.406

5.  Brief clinical report: ring chromosome 17 in a mentally retarded young man - clinical, cytogenetic, and biochemical investigations.

Authors:  A E Chudley; P D Pabello; P J McAlpine; B E Nickel; M H Shokeir
Journal:  Am J Med Genet       Date:  1982-06

6.  An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?

Authors:  N J Carpenter; L G Leichtman; S Stamper; B Say
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

7.  Partial deletion of distal 17q.

Authors:  J Bridge; W Sanger; G Mosher; B Buehler; R Nelson; M Welsh; J Newland; M Kafka
Journal:  Am J Med Genet       Date:  1985-06

8.  The MIller-Dieker syndrome.

Authors:  K L Jones; E F Gilbert; E G Kaveggia; J M Opitz
Journal:  Pediatrics       Date:  1980-08       Impact factor: 7.124

9.  Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.

Authors:  P vanTuinen; W B Dobyns; D C Rich; K M Summers; T J Robinson; Y Nakamura; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

10.  New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13.

Authors:  R F Stratton; W B Dobyns; S D Airhart; D H Ledbetter
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

View more
  4 in total

1.  Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisation.

Authors:  H M Kingston; D H Ledbetter; P I Tomlin; K L Gaunt
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

Review 2.  Genetic factors in lissencephaly syndromes: a review.

Authors:  P Miny; W Holzgreve; J Horst
Journal:  Childs Nerv Syst       Date:  1993-11       Impact factor: 1.475

3.  Miller-Dieker syndrome with der(17)t(12;17)(q24.33;p13.3)pat presenting with a potential risk of mis-identification as a de novo submicroscopic deletion of 17p13.3.

Authors:  Young Jin Kim; Shin Yun Byun; Seon A Jo; Yong Beom Shin; Eun Hae Cho; Eun Yup Lee; Sang-Hyun Hwang
Journal:  Korean J Lab Med       Date:  2011-01

Review 4.  Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3.

Authors:  Sara M Blazejewski; Sarah A Bennison; Trevor H Smith; Kazuhito Toyo-Oka
Journal:  Front Genet       Date:  2018-03-23       Impact factor: 4.599

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.