A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome

A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome

Background: 47 XXY/46 XX mosaicism with characteristics suggesting Klinefelter syndrome is very rare and at present, only seven cases have been reported in the literature.

Bibliographic Details
Main Authors: Jalaludin, MY (Author), Nor, NSM (Author)
Format: Article
Language:English
Published: 2016
Subjects:
47XXY/46XX mosaicism
KARYOTYPE
Klinefelter syndrome
OVULATION
PHENOTYPIC MALE
Radioulnar synostosis
RADIOULNAR SYNOSTOSIS
TRUE HERMAPHRODITISM
Online Access:View Fulltext in Publisher
Description
Summary:Background: 47 XXY/46 XX mosaicism with characteristics suggesting Klinefelter syndrome is very rare and at present, only seven cases have been reported in the literature.
DOI:10.1186/s13633-016-0029-3

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