
XXYY syndrome - Wikipedia
XXYY syndrome is a sex chromosome anomaly in which males have two extra chromosomes, one X and one Y chromosome. Human cells usually contain two sex chromosomes, one from …
What is XXYY Syndrome? - The Association for X and Y …
XXYY Syndrome is the name attached to the cluster of symptoms that arise as a result of the 48,XXYY chromosome pattern. It affects one in every 17,000 boys.
48, XXYY Syndrome - Symptoms, Causes, Treatment | NORD
2022年3月24日 · 48, XXYY is a genetic disorder that occurs in males and is characterized by additional sex chromosomes compared to the typical male karyotype of 46, XY. 48, XXYY …
XXYY syndrome - Simple English Wikipedia, the free encyclopedia
XXYY syndrome is a rare genetic disorder. Usually, a male will have one X chromosome and one Y chromosome , but people with this disorder have two of each. They have 48 chromosomes …
48,XXYY syndrome - MedlinePlus
48,XXYY syndrome is a chromosomal condition that affects male development. There is a lot of variability in symptoms between people with 48,XXYY syndrome. Almost all affected …
48,XXYY syndrome | About the Disease | GARD - Genetic and Rare …
48,XXYY syndrome is a chromosomal condition, characterized by the presence of an extra X and Y chromosome in males, that causes medical and behavioral problems. 48,XXYY can be …
About 48,XXYY - The Association for X and Y Chromosome Variations
Our vision is a world where men and boys with XXYY Syndrome lead purposeful, productive lives. Read more about our mission. What is XXYY Syndrome? In support of our mission, the XXYY …
What Is 48, XXYY Syndrome? - iCliniq
2023年11月14日 · 48, XXYY syndrome is a rare genetic condition, sometimes called double Y syndrome. Males are commonly affected. It is distinguished by an additional X and Y …
XXYY syndrome (Concept Id: C2936741) - National Center for ...
Macular hypoplasia and high myopia in 48, xxyy syndrome: a unique case of 48, xxyy syndrome that presents with high myopia and macular dysplasia.
Orphanet: 48,XXYY syndrome
A rare sex chromosome number anomaly disorder characterized, genetically, by the presence of an extra X and Y chromosome in males and, clinically, by tall stature, dysfunctional testes …
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