Xxx syndrome karyotype

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Triple X syndromealso known as trisomy X and 47,XXXis characterized by the presence of an extra X chromosome in each cell of a female. Triple X is due to a random event. Treatment may include speech therapy, physical therapy, and counseling.

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Received Date: Triple X syndrome trisomy X is a sex chromosomal anomaly caused by the presence of an extra X chromosome. The patients with Triple X syndrome have a wide range of phenotypic variability.

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A description of their growth and development is presented. The birth weight was normal in all patients and one of them had facial dysmorphism with right microphtalmia and auricular septal defect. During the first 2 years of life, the neuromotor development of these infants was not distinguishable from chromosomally normal children.

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Triple X syndromealso called trisomy X or 47,XXX, is characterized by the presence of an additional X chromosome in each of a female's cells. Although females with this condition may be taller than average, this chromosomal change typically causes no unusual physical features. Most females with triple X syndrome have normal sexual development and are able to conceive children.

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Triple X syndrome is a genetic condition found in females only. About 1 in 1, girls have it. Other symptoms can include problems with spoken language and processing spoken words, coordination problems, and weaker muscles.

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MIFTS : Expand all tables. Xxx Syndrome 54 26

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Anthony M. Clinical Genetics. Molecular Genetics. Address for correspondence.

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Metrics details. Trisomy X is a sex chromosome anomaly with a variable phenotype caused by the presence of an extra X chromosome in females 47,XXX instead of 46,XX. It is the most common female chromosomal abnormality, occurring in approximately 1 in 1, female births.

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The symptoms and physical features associated with trisomy X vary greatly from one person to another. Some females may have no symptoms asymptomatic or very mild symptoms and may go undiagnosed. Other women may have a wide variety of different abnormalities.

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