Open AccessRare 48, XYYY syndrome: case report and review of the literature
Author(s) -
Abedi Maryam,
Salmaninejad Arash,
Sakhinia Ebrahim
Publication year - 2018
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.1311
Subject(s) - medicine , short stature , klinefelter syndrome , deformity , pediatrics , tall stature , dermatology , bioinformatics , surgery , biology
Key Clinical Message 48, XYYY syndrome is a rare condition. A male with 32‐year‐old and three Y chromosomes is described. This syndrome is phenotypically similar to Klinefelter syndrome. In this patient, Semi‐Klinefelter characteristics such as tall stature, teeth dysmorphology, long length of fingers, partial deformity of the joints, likewise mental health problems were obvious.