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Eruption delay in a 47 XXY male: a case report
G D'Alessandro1, L Armuzzi, G Cocchi
1Department of Dental Science, Dental School, Alma Mater Studiorum, University of Bologna, Bologna, Italy. dr.dalessandro@gmail.com
European Journal of Paediatric Dentistry
|July 6, 2012
Summary
Klinefelter syndrome (47,XXY) is the most common sex chromosome disorder in males. This case highlights a potential link between Klinefelter syndrome and delayed primary tooth eruption in infants.
Area of Science:
- Genetics
- Pediatrics
- Endocrinology
Background:
- 47,XXY syndrome, also known as Klinefelter syndrome, is the most frequent sex chromosome abnormality in males.
- It is often underdiagnosed and typically identified after puberty, but prenatal diagnosis is possible via chorionic villus sampling.
Observation:
- A 16-month-old Italian male with 47,XXY syndrome presented with delayed primary tooth eruption (8-10 months).
- Auxological development (weight and height) was normal, around the 50th percentile, during the first 15 months of life.
Findings:
- The observed delay in primary teeth eruption in this infant with Klinefelter syndrome suggests a potential association.
- Sexual chromosomes are implicated in influencing dental development, warranting further investigation.
Implications:
- This case suggests a possible correlation between Klinefelter syndrome and delayed dental development, even with normal overall growth.
- Early identification of such dental anomalies may aid in the earlier diagnosis of Klinefelter syndrome.
- Further research is needed to confirm the role of sex chromosomes in dental development delays associated with 47,XXY syndrome.
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The Y Chromosome Determines Maleness
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Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size. Today,...
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