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Chromosome Disorder Leaflets

We have been collecting information about specific chromosome disorders in our comprehensive offline database for nearly 25 years and since 2003 have spent many thousands of hours producing family-friendly, medically-verified, disorder-specific information leaflets. These leaflets are dynamic documents and will be updated as new information becomes available. New leaflets about other chromosome disorders will be coming on stream all the time. To find out about the exacting process we adopted to produce these leaflets, please view our leaflet protocol description.

We have produced two levels of information leaflet about many of the rare chromosomal disorders affecting our members (see the table below for the specific titles), including:

Just click on the relevant title in the table below to download the Unique Information Leaflets on the disorders in which you are interested.

Whether you are a family or professional or a member of the general public, please help us to continue this work by being generous with your donations, fundraising or sponsorship. We receive no government funding and can only continue our work with your support. If you are a family affected by a rare chromosome disorder, please do join us and contribute to the collective knowledge so that we can continue to make our leaflets even more comprehensive.

Before downloading any of our leaflets, we ask you to please read and adhere to our disclaimer and copyright notice.




Title Web Version Print Version Quick Read Other Versions
Chromosome 1  
1p interstitial deletions Web Version
 Print Version
    
1p36 deletion Web Version
 Print Version
    
1p36 deletion French     Quick Read
  
1p36 deletion Polish Web Version
      
1p36 deletion     Quick Read
  
1p36 deletion Spanish Web Version
 Print Version
    
1p36 deletions Polish   Print Version
    
1q21.1 microdeletions Web Version
 Print Version
    
1q21.1 microdeletions Polish Web Version
 Print Version
    
1q21.1 microdeletions Spanish Web Version
 Print Version
    
1q21.1 microduplications Web Version
 Print Version
    
1q4 deletions Web Version
 Print Version
 Quick Read
  
Duplications of 1q Web Version
 Print Version
    
Supernumerary ring chromosome 1 Web Version
 Print Version
    
Chromosome 2  
2p deletions Web Version
 Print Version
    
2p15p16.1 microdeletion syndrome Web Version
 Print Version
    
2q24.3 deletions Web Version
 Print Version
    
2q32 deletions and microdeletions Web Version
 Print Version
    
2q32 deletions and microdeletions French Web Version
 Print Version
    
2q33.1 deletions and other deletions between 2q31 and 2q33 Web Version
 Print Version
    
2q37 deletion syndrome Web Version
 Print Version
    
2q37 deletions French     Quick Read
  
2q37 deletions     Quick Read
  
2q37 deletions adults adolescents Web Version
 Print Version
    
Duplications of 2p Web Version
 Print Version
    
Duplications of 2q Web Version
 Print Version
    
Ring 2 Web Version
 Print Version
 Quick Read
  
Chromosome 3  
3p25 deletions Web Version
 Print Version
    
3p25 deletions German Web Version
 Print Version
    
3p25 deletions     Quick Read
  
3p25 deletions Spanish Web Version
 Print Version
    
3q29 Duplications and Microduplications Web Version
 Print Version
    
3q29 deletions and microdeletions Web Version
 Print Version
    
Duplications of 3q Web Version
 Print Version
    
Chromosome 4  
4p 8p Translocation Web Version
 Print Version
    
4p Duplications Web Version
 Print Version
 Quick Read
  
4q deletions between 4q11 and 4q22 Web Version
 Print Version
    
4q deletions between 4q21 and 4q22 Web Version
 Print Version
    
4q deletions between 4q21 and 4q22 German Web Version
 Print Version
    
4q deletions between 4q21 and 4q31 Web Version
 Print Version
    
4q deletions from 4q31 and beyond Web Version
 Print Version
    
Duplications of 4q Web Version
 Print Version
    
Chromosome 5  
5q deletions including 5q22 Web Version
 Print Version
 Quick Read Print
Quick Read Web
  
5q14.3 deletions Web Version
 Print Version
    
Deletions including 5q22 French     Quick Read
  
Chromosome 6  
6p deletions Web Version
 Print Version
 Quick Read
  
6q deletions 6q11 to 6q16 Web Version
 Print Version
    
6q deletions 6q13 to 6q14 Web Version
 Print Version
    
6q deletions 6q15 to 6q23 Web Version
 Print Version
    
6q deletions 6q15 to 6q23 German Web Version
 Print Version
    
6q deletions from 6q23 to 6q24 Web Version
 Print Version
    
6q deletions from 6q25 Web Version
 Print Version
    
6q deletions from 6q26 and 6q27 Web Version
 Print Version
    
Duplications of 6p Web Version
 Print Version
    
Duplications of 6q Web Version
 Print Version
    
Chromosome 7  
7q deletions between 7q21 7q32 Web Version
 Print Version
    
7q deletions proximal interstitial Web Version
 Print Version
    
7q duplications Web Version
 Print Version
 Quick Read
  
7q11.23 duplications Web Version
 Print Version
    
7q11.23 microduplications Spanish Web Version
 Print Version
    
7q32q34 Deletions Web Version
 Print Version
    
7q36 deletions Web Version
 Print Version
    
7q36 deletions German Web Version
 Print Version
    
7q36 deletions     Quick Read Print
Quick Read Web
  
Duplications of 7q Spanish Web Version
 Print Version
    
Chromosome 8  
4p 8p Translocation Web Version
 Print Version
    
8p duplications Web Version
 Print Version
    
8p duplications French     Quick Read
  
8p duplications     Quick Read
  
8p inv dup del Web Version
 Print Version
 Quick Read
  
8p23 deletions Web Version
 Print Version
 Quick Read
  
8p23 duplications Web Version
 Print Version
    
8q duplications Web Version
 Print Version
 Quick Read
  
Inv dup del 8p French     Quick Read
  
Supernumerary chromosome 8 Web Version
 Print Version
    
Trisomy 8 Mosaicism Web Version
 Print Version
    
Trisomy 8 Mosaicism French     Quick Read
  
Trisomy 8 Mosaicism     Quick Read
  
Trisomy 8 mosaicism German Web Version
 Print Version
    
Trisomy 8 mosaicism in adults Web Version
 Print Version
    
Chromosome 9  
9p deletions Dutch Web Version
 Print Version
    
9p deletions Web Version
 Print Version
    
9p deletions French     Quick Read
  
9p deletions     Quick Read
  
9p24 deletions Web Version
 Print Version
    
9q34 duplication syndrome Web Version
 Print Version
    
Duplications of 9p Web Version
 Print Version
    
Duplications of 9p German Web Version
 Print Version
    
Duplications of 9p Spanish Web Version
 Print Version
    
Kleefstra Syndrome Web Version
 Print Version
    
Ring 9 Web Version
 Print Version
    
Tetrasomy 9p Web Version
 Print Version
    
Trisomie 9 en mosaique     Quick Read
  
Trisomy 9 mosaicism Web Version
 Print Version
 Quick Read
  
Trisomy 9 mosaicism German     Quick Read
  
Trisomy 9 mosaicism Spanish Web Version
 Print Version
    
Chromosome 10  
10p deletions Web Version
 Print Version
    
10q22q24 deletions Web Version
 Print Version
    
10q25 and 10q26 deletions Web Version
 Print Version
 Quick Read
  
10q26 deletions French     Quick Read
  
Duplications of 10p Web Version
 Print Version
    
Duplications of 10q Web Version
 Print Version
    
Chromosome 11  
11 22 Translocation Web Version
 Print Version
    
11q deletion disorder Jacobsen syndrome Web Version
 Print Version
    
Emanuel syndrome Web Version
 Print Version
    
Jacobsen Dutch Web Version
      
Jacobsen French Web Version
 Print Version
    
Jacobsen Spanish Web Version
 Print Version
    
Jacobsen Syndrome German Web Version
 Print Version
    
Chromosome 12  
12q deletions Web Version
 Print Version
    
12q14 microdeletion Web Version
 Print Version
    
Duplications of 12p Web Version
 Print Version
    
Pallister Killian French     Quick Read
  
Pallister-Killian syndrome Web Version
 Print Version
 Quick Read
  
Chromosome 13  
13q deletions including RB1 Web Version
 Print Version
    
13q deletions various Web Version
 Print Version
    
13q deletions various German Web Version
 Print Version
    
13q distal interstitial deletions Web Version
 Print Version
    
Deletions including the end of 13q Web Version
 Print Version
    
Deletions including the end of 13q French Web Version
 Print Version
    
Ring 13 Web Version
 Print Version
 Quick Read
  
Chromosome 14  
14q deletions between 14q22 14q32 Web Version
 Print Version
    
14q deletions from 14q31 and 14q32.1 Web Version
 Print Version
    
14q deletions from 14q32.2 and 14q32.3 Web Version
 Print Version
    
14q deletions proximal to 14q22 Web Version
 Print Version
    
Duplications of 14q distal Web Version
 Print Version
    
Ring 14 Web Version
 Print Version
    
Ring 14 French     Quick Read
  
Ring 14     Quick Read
  
Trisomy 14 mosaicism Web Version
 Print Version
    
UPD 14 Web Version
 Print Version
 Quick Read
  
Chromosome 15  
15q Deletions Web Version
 Print Version
    
15q11 2 microdeletions Web Version
 Print Version
    
15q13.3 microdeletion syndrome Web Version
 Print Version
    
15q24 microdeletion syndrome Web Version
 Print Version
    
Duplications of 15q Web Version
 Print Version
    
Idic 15 French     Quick Read
  
Idic 15 German     Quick Read
  
Idic 15     Quick Read
  
Idic(15) Italian Web Version
 Print Version
    
Idic15 Web Version
 Print Version
    
Ring 15 Web Version
 Print Version
    
Ring 15 French     Quick Read
  
Ring 15     Quick Read
  
Chromosome 16  
16p proximal deletions Web Version
 Print Version
    
16p11.2 microdeletions Web Version
 Print Version
    
16p11.2 microdeletions Spanish Web Version
 Print Version
    
16p11.2 microduplications Web Version
 Print Version
    
16p13 deletions Web Version
 Print Version
    
16p13.11 microdeletions Web Version
 Print Version
    
16p13.11 microduplications Web Version
 Print Version
    
16q Deletions Web Version
 Print Version
    
Duplications of 16p Web Version
 Print Version
    
Duplications of proximal 16q Web Version
 Print Version
    
Trisomy 16 Mosaicism Web Version
 Print Version
    
Trisomy 16 Mosaicism Stories Web Version
      
Chromosome 17  
17p duplications French     Quick Read
  
17p13 1 and 17p13 2 microdeletions Web Version
 Print Version
    
17q12 microdeletions Web Version
 Print Version
    
17q12 microdeletions Spanish Web Version
 Print Version
    
17q21.31 microdeletions French Web Version
 Print Version
    
17q21.31 microdeletions Spanish Web Version
 Print Version
    
Duplications of 17p Web Version
 Print Version
 Quick Read
  
Koolen-De Vries Syndrome Web Version
 Print Version
    
Chromosome 18  
18p deletions Web Version
 Print Version
    
18p deletions Italian Web Version
 Print Version
    
18q deletions from 18q11 2 to 18q21 2 Italian Web Version
 Print Version
    
18q deletions from 18q11 2 to 18q21 2 Spanish Web Version
 Print Version
    
18q deletions from 18q11.2 to 18q21.2   Print Version
    
18q deletions from 18q11.2 to 18q21.2 Web Version
      
18q deletions from 18q21 and beyond   Print Version
    
18q deletions from 18q21 and beyond Italian Web Version
 Print Version
    
18q deletions from18q21and beyond Web Version
      
Ring 18 Web Version
 Print Version
    
Ring 18 French     Quick Read
  
Ring 18 German Web Version
 Print Version
    
Ring 18     Quick Read
  
Chromosome 19  
         
Chromosome 20  
20p deletions Web Version
 Print Version
    
Duplications of 20p Web Version
 Print Version
    
Duplications of 20p German Web Version
 Print Version
    
Ring 20 Web Version
 Print Version
    
Chromosome 21  
21q deletions Web Version
 Print Version
 Quick Read
  
Ring 21 Web Version
 Print Version
 Quick Read
  
Chromosome 22  
11 22 Translocation Web Version
 Print Version
    
22q11.2 deletions syndrome (Velo-Cardio-Facial Syndrome) Web Version
 Print Version
    
22q11.2 distal deletion syndrome Web Version
 Print Version
    
22q11.2 duplications Web Version
 Print Version
    
22q12q13 duplications Web Version
 Print Version
    
22q13 deletion French     Quick Read
  
22q13 deletion Spanish     Quick Read
  
22q13 deletions Dutch Web Version
 Print Version
    
22q13 deletions Web Version
 Print Version
 Quick Read
  
Emanuel syndrome Web Version
 Print Version
    
Ring 22 Web Version
 Print Version
    
Ring 22 French     Quick Read Print
Quick Read Web
  
Ring 22 German Web Version
 Print Version
    
Ring 22     Quick Read Print
Quick Read Web
  
Chromosome X  
Pentasomy X Web Version
 Print Version
 Quick Read
  
Pentasomy X German Web Version
 Print Version
    
Tetrasomie X Web Version
 Print Version
    
Tetrasomy X Web Version
 Print Version
 Quick Read
  
Tetrasomy X Dutch Web Version
 Print Version
    
Triple X Web Version
 Print Version
    
Triple X Danish Web Version
 Print Version
    
Triple X Spanish Web Version
 Print Version
    
XXXXY Web Version
 Print Version
 Quick Read
  
XXXXY syndrome Spanish Web Version
 Print Version
    
XXXXY syndrome French Web Version
 Print Version
 Quick Read
  
XXXY syndrome Spanish Web Version
 Print Version
    
XXXY syndrome Web Version
 Print Version
    
XXXY syndrome French Web Version
 Print Version
    
XXYY French     Quick Read
  
XXYY syndrome Web Version
 Print Version
 Quick Read
  
Xp11.2 duplications Web Version
 Print Version
    
Xq28 duplications Web Version
 Print Version
    
Chromosome Y  
45X 46XY including Y chromosome rearrangements   Print Version
    
45X 46XY including Y chromosome rearrangements Web Version
      
XXYY French     Quick Read
  
XXYY syndrome Web Version
 Print Version
 Quick Read
  
XYY Web Version
 Print Version
    
XYY German Web Version
 Print Version
    
XYY     Quick Read
  
XYYY     Quick Read
  
XYYY syndrome Web Version
 Print Version
    
Other  
4q- Parents Perspective       paper
After Diagnosis Web Version
 Print Version
    
Array CGH Arabic     Quick Read
  
Array CGH Danish     Quick Read
  
Array CGH Web Version
 Print Version
    
Array CGH French     Quick Read
  
Array CGH Greek     Quick Read
  
Array CGH Italian     Quick Read
  
Array CGH     Quick Read
  
Array CGH Romanian     Quick Read
  
Array CGH Spanish     Quick Read
  
Balanced Translocations Greek Web Version
 Print Version
    
Balanced Translocations Spanish Web Version
 Print Version
    
Balanced translocations Web Version
 Print Version
    
Diploid triploid Children     Quick Read
  
Diploidy triploidy Web Version
 Print Version
    
FISH Web Version
 Print Version
 Quick Read
  
Grants and funding guide Web Version
 Print Version
    
Holidays short breaks travel guide Web Version
 Print Version
    
Outdoor bikes leisure and sensory toys Web Version
 Print Version
    
Robertsonian Translocations Web Version
 Print Version
    
Robertsonian Translocations German Web Version
 Print Version
    
Small supernumerary marker chromosomes (sSMC) Web Version
 Print Version
    
Small supernumerary marker chromosomes (sSMC) German Web Version
 Print Version
    
Supporting Siblings of Children with a Rare Chromosome Disorder Web Version
 Print Version
    
Triploid Pregnancies     Quick Read Print
  
Triploidy Web Version
 Print Version
    
Reports  
1p36 study day report Web Version
      
2q37 Deletion Study Weekend Report Web Version
      
4q Deletions Study Weekend       report
8p23 Deletions and Inv Dup Del 8p Study Weekend       report
Kleefstra Syndrome Study Weekend Report Web Version
      
Pallister Killian Syndrome Study Weekend       report
XXX Study Day Report Web Version
      
XYY Study Day Report Web Version
      

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Website last updated on 20 May 2013 Copyright © 1996-2013 Unique You are visitor number 2384159
This page last updated 16 May 2013 The Rare Chromosome Disorder Support Group There have been 314761 visits to this page
Website editor Beverly Searle BSc(Hons) PhD CBiol MSB