Literature DB >> 12712270

Paternal uniparental disomy 14: introducing the "coat-hanger" sign.

Amaka C Offiah1, Luc Cornette, Christine M Hall.   

Abstract

Paternal uniparental disomy for chromosome 14 (patUPD14) is a rare condition, this being the eighth report. A male infant, born prematurely, was noted to have extremely lax skin and bilateral inguinal hernias. Skin biopsy confirmed the clinical diagnosis of congenital cutis laxa, but this did not explain the limb abnormalities. Radiographic findings (particularly the "coat-hanger" configuration of the ribs on the chest radiograph), suggested a diagnosis of patUPD14, which was confirmed following DNA analysis. The patient died after prolonged respiratory failure. This combination of patUPD14 and congenital cutis laxa has not previously been described. Radiology can play a pivotal role in guiding the geneticist's choice of investigation.

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Year:  2003        PMID: 12712270     DOI: 10.1007/s00247-003-0931-8

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  14 in total

1.  International nosology and classification of constitutional disorders of bone (2001).

Authors:  Christine M Hall
Journal:  Am J Med Genet       Date:  2002-11-15

2.  Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier.

Authors:  J C Wang; M B Passage; P H Yen; L J Shapiro; T K Mohandas
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

Review 3.  The lethal osteochondrodysplasias.

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Journal:  Adv Hum Genet       Date:  1990

Review 4.  Uniparental disomy (UPD). Genomic imprinting and a case for new genetics (prenatal and clinical implications: the "Likon" concept).

Authors:  E Engel
Journal:  Ann Genet       Date:  1997

5.  Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11).

Authors:  C A Walter; L G Shaffer; C I Kaye; R W Huff; P D Ghidoni; C McCaskill; M B McFarland; C M Moore
Journal:  Am J Med Genet       Date:  1996-11-11

6.  Facial anomalies in congenital cutis laxa with retarded growth and skeletal dysplasia.

Authors:  L Van Maldergem; G Ogŭr; M Yüksel
Journal:  Am J Med Genet       Date:  1989-02

7.  Human elastin gene: new evidence for localization to the long arm of chromosome 7.

Authors:  M J Fazio; M G Mattei; E Passage; M L Chu; D Black; E Solomon; J M Davidson; J Uitto
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

8.  A new genetic concept: uniparental disomy and its potential effect, isodisomy.

Authors:  E Engel
Journal:  Am J Med Genet       Date:  1980

Review 9.  Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

Authors:  P R Papenhausen; O T Mueller; V P Johnson; M Sutcliffe; T M Diamond; B G Kousseff
Journal:  Am J Med Genet       Date:  1995-11-20

10.  Paternal UPD14 is responsible for a distinctive malformation complex.

Authors:  Kenji Kurosawa; Hiroyuki Sasaki; Yoshiaki Sato; Michiko Yamanaka; Mitsumasa Shimizu; Yuji Ito; Torayuki Okuyama; Mari Matsuo; Kiyoshi Imaizumi; Yoshikazu Kuroki; Gen Nishimura
Journal:  Am J Med Genet       Date:  2002-07-01
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  9 in total

1.  Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion.

Authors:  Sami Tsukishiro; Qing Ying Li; Mitsuyo Tanemura; Mayumi Sugiura-Ogasawara; Kaoru Suzumori; Shin-Ichi Sonta
Journal:  J Hum Genet       Date:  2005-03-04       Impact factor: 3.172

2.  Paternal uniparental disomy of chromosome 14.

Authors:  K M Sargar; T E Herman; M J Siegel
Journal:  J Perinatol       Date:  2014-09       Impact factor: 2.521

3.  Radiological evaluation of dysmorphic thorax of paternal uniparental disomy 14.

Authors:  Osamu Miyazaki; Gen Nishimura; Masayo Kagami; Tsutomu Ogata
Journal:  Pediatr Radiol       Date:  2011-05-24

4.  Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14.

Authors:  Melita D Irving; Karin Buiting; Deniz Kanber; Celia Donaghue; Reiner Schulz; Amaka Offiah; Shehla N Mohammed; Rebecca J Oakey
Journal:  Am J Med Genet A       Date:  2010-08       Impact factor: 2.802

Review 5.  Genomic imprinting of the type 3 thyroid hormone deiodinase gene: regulation and developmental implications.

Authors:  Marika Charalambous; Arturo Hernandez
Journal:  Biochim Biophys Acta       Date:  2012-04-04

6.  Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.

Authors:  Laura K Conlin; Brian D Thiel; Carsten G Bonnemann; Livija Medne; Linda M Ernst; Elaine H Zackai; Matthew A Deardorff; Ian D Krantz; Hakon Hakonarson; Nancy B Spinner
Journal:  Hum Mol Genet       Date:  2010-01-06       Impact factor: 6.150

7.  Kagami-Ogata Syndrome: Case Series and Review of Literature.

Authors:  Rishika P Sakaria; Roya Mostafavi; Stephen Miller; Jewell C Ward; Eniko K Pivnick; Ajay J Talati
Journal:  AJP Rep       Date:  2021-05-27

8.  Uniparental disomy and prenatal phenotype: Two case reports and review.

Authors:  Xiaofei Li; Yan Liu; Song Yue; Li Wang; Tiejuan Zhang; Cuixia Guo; Wenjie Hu; Karl-Oliver Kagan; Qingqing Wu
Journal:  Medicine (Baltimore)       Date:  2017-11       Impact factor: 1.817

9.  Anesthetic management of a child with Kagami-Ogata syndrome complicated with marked tracheal deviation: a case report.

Authors:  Kazuaki Yamagata; Atsushi Kawamura; Satomi Kasai; Mai Akazawa; Michiru Takeda; Kazuya Tachibana
Journal:  JA Clin Rep       Date:  2018-08-31
  9 in total

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