Document Detail


Eruption delay in a 47 XXY male: a case report.
MedLine Citation:
PMID:  22762182     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: The 47,XXY syndrome, or Klinefelter syndrome, though it is a rare occurrence, it is the most common sex choromosome disorder affecting male subjects. This syndrome is underdiagnosed and seldomly before puberty. In this case, diagnosis was made before birth, through chorion villus sampling.
CASE REPORT: A 16 month-old Italian male with 47 XXY syndrome showed the absence of primary teeth, with a delay of about 8-10 months, whereas during the first 15 months of life the auxological development has been normal both in weight and height (about 50th percentile). We assumed that this delay may be linked with Klinefelter syndrome, as sexual chromosomes play an important role in the dental development.
Authors:
G D'Alessandro; L Armuzzi; G Cocchi; G Piana
Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry     Volume:  13     ISSN:  1591-996X     ISO Abbreviation:  Eur J Paediatr Dent     Publication Date:  2012 Jun 
Date Detail:
Created Date:  2012-07-05     Completed Date:  2012-10-24     Revised Date:  2013-05-20    
Medline Journal Info:
Nlm Unique ID:  101121881     Medline TA:  Eur J Paediatr Dent     Country:  Italy    
Other Details:
Languages:  eng     Pagination:  159-60     Citation Subset:  D; IM    
Affiliation:
Department of Dental Science, Dental School, Alma Mater Studiorum, University of Bologna, Bologna, Italy. dr.dalessandro@gmail.com
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MeSH Terms
Descriptor/Qualifier:
Body Height
Body Weight
Follow-Up Studies
Humans
Infant
Klinefelter Syndrome / physiopathology*
Male
Tooth Eruption / physiology*
Tooth, Deciduous / physiopathology*

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