Template:Chromosome Aneuploidy table: Difference between revisions

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* '''{{trisomy 21}}''' - Down syndrome
* '''{{trisomy 21}}''' - {{Down syndrome}}
* '''{{trisomy 18}}''' - Edwards syndrome
* '''{{trisomy 18}}''' - {{Edwards syndrome}}
* '''{{trisomy 13}}''' - Patau syndrome
* '''{{trisomy 13}}''' - {{Patau syndrome}}
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* {{monosomy X}} - Turner's syndrome
* '''{{monosomy X}}''' - {{Turner's syndrome}}
* {{trisomy X}} - Triple-X syndrome
* '''{{trisomy X}}''' - {{Triple-X syndrome}}
* {{47 XXY}} - {{Klinefelter syndrome}}
* '''{{47 XXY}}''' - {{Klinefelter syndrome}}
* {{47 XYY}} - {{Jacob's syndrome}}  
* '''{{47 XYY}}''' - {{Double Y syndrome}}  
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XYY syndrome is a rare chromosomal disorder caused by the presence of an extra Y chromosome. Normally, males have 46 chromosomes including one X and one Y chromosome. Males with XYY syndrome have 47 chromosomes, two of which are Y chromosomes.
902599592
LD52.1 Male with double or multiple Y
Parent
LD52 Number anomalies of chromosome Y
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Description
A condition affecting males, caused by the presence of supernumerary Y chromosomes. This condition is asymptomatic. Confirmation is through observation of supernumerary Y chromosomes by karyotyping.

Latest revision as of 11:39, 8 May 2019