Literature DB >> 20672182

[Phenotypic variability in 47, XXX patients: Clinical report of four new cases].

Ernesto Goldschmidt1, Marisa Márquez, Andrea Solari, María I Ziembar, Alejandro Laudicina.   

Abstract

The 47, XXX karyotype has a frequency of 1 in 1000 female newborns. However, this karyotype is not usually suspected at birth or childhood. These patients are usually diagnosed during adulthood when they develop premature ovarian failure or infertility, because the early phenotype doesn t have any specific features. The study describes four cases and the clinical variability of the 47, XXX karyotype.

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Year:  2010        PMID: 20672182     DOI: 10.1590/S0325-00752010000400012

Source DB:  PubMed          Journal:  Arch Argent Pediatr        ISSN: 0325-0075            Impact factor:   0.635


  1 in total

1.  Triple X Egyptian woman and a Down's syndrome offspring.

Authors:  Faeza Abdel Mogib El-Dahtory
Journal:  Indian J Hum Genet       Date:  2013-01
  1 in total

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