Rare 48, XYYY syndrome: case report and review of the literature

Abedi, M. and Salmaninejad, A. and Sakhinia, E. (2018) Rare 48, XYYY syndrome: case report and review of the literature. Clinical Case Reports, 6 (1). pp. 179-184.

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Abstract

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. © 2017 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Item Type: Article
Additional Information: Export Date: 16 February 2020 Correspondence Address: Sakhinia, E.; Connective Tissue Research Center, Department of Medical Genetics, Faculty of Medicine and Tabriz Genetic Analysis Centre (TGAC), Tabriz University of Medical SciencesIran; email: esakhinia@yahoo.co.uk
Uncontrolled Keywords: 48, XYYY syndrome chromosomal abnormality cytogenetic QF-PCR sex chromosome 48,xyyy syndrome adult Article asthma azoospermia birth weight body mass case report chest infection chromatid aberration chromosome disorder clinical article coughing cytogenetics deformity human karyotyping learning disorder male male infertility mental health mental instability muscle tone polymerase chain reaction priority journal speech delay spermiogram teratology
Subjects: QU Biochemistry
QZ pathology-neoplasms-Genetics
Divisions: Mashhad University of Medical Sciences
Depositing User: lib2 lib2 lib2
Date Deposited: 10 Jun 2020 06:59
Last Modified: 10 Jun 2020 06:59
URI: http://eprints.mums.ac.ir/id/eprint/17164

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