46, XX testicular disorder of sex development (DSD): a case report and systematic review

M Terribile, M Stizzo, C Manfredi, C Quattrone… - Medicina, 2019 - mdpi.com
Background and objectives: XX male syndrome is part of the disorders of sex development
(DSD). The patients generally have normal external genitalia and discover their pathology in …

Chromosome abnormalities and fertility in domestic bovids: A review

A Iannuzzi, P Parma, L Iannuzzi - Animals, 2021 - mdpi.com
Simple Summary In domestic bovids, numerical autosome abnormalities have been rarely
reported, as they present abnormal animal phenotypes quickly eliminated by breeders …

46 XX karyotype during male fertility evaluation; case series and literature review

A Majzoub, M Arafa, C Starks, H Elbardisi… - Asian journal of …, 2017 - journals.lww.com
Forty-six XX disorder of sex development is an uncommon medical condition observed at
times during the evaluation of a man's fertility. The following is a case series and literature …

Disorders of sexual development and abnormal early development in domestic food-producing mammals: the role of chromosome abnormalities, environment and …

LA Favetta, DAF Villagómez, L Iannuzzi, G Di Meo… - Sexual …, 2012 - karger.com
The management of disorders of sexual development (DSD) in humans and domestic
animals has been the subject of intense interest for decades. The association between …

A 46, XX karyotype in men with infertility: Two new cases and review of the literature

E Kouvidi, H Tsimela, L Lazaros… - Journal of Human …, 2022 - journals.lww.com
Abstract 46, XX male sex reversal syndrome is a rare genetic cause of male infertility. We
report on two new cases of this syndrome in men presenting with hypogonadism and …

[HTML][HTML] Chromosomal aneuploidies and associated rare genetic syndromes involved in male infertility

ET Marzouni, AB Harchegani, I Layali - 2021 - jomh.org
Background and objectives: Recent investigations have reported more than 70 genetic
syndromes involved in male infertility; however, the majority of these syndromes are …

[HTML][HTML] Cytogenetic investigation in a group of ten infertile men with non-obstructive azoospermia: First Algerian 46, xx syndrome

M Baziz, Z Hamouli-Said, I Ratbi, M Habel… - Iranian Journal of …, 2016 - ncbi.nlm.nih.gov
Background: In Algeria, the data on infertility and its various causes are rare. Recently, the
introduction of assisted reproduction has allowed expecting that 300000 couples, which …

Extinction of chromosomes due to specialization is a universal occurrence

J Wilson, JM Staley, GJ Wyckoff - Scientific Reports, 2020 - nature.com
The human X and Y chromosomes evolved from a pair of autosomes approximately 180
million years ago. Despite their shared evolutionary origin, extensive genetic decay has …

[PDF][PDF] COMPLETE SEX REVERSAL: SRY POSITIVE 46, XX MALE BY Y TO X TRANSLOCATION.

C Procopiuc, C Dumitrescu, C Chirita… - Acta Endocrinologica …, 2009 - academia.edu
Individuals with male phenotypes and 46 XX karyotype appear in about 1 of 20,000 births
with clinical features varying from normal male appearance to sexual ambiguity and …

A rare genetic gender anomaly identified in a paternity case presenting AMEL-Y dropout

RA Nicolae, AM Constantinescu, AC Costea… - Forensic Science …, 2019 - Elsevier
The examination of different sets of sex markers in view of gender determination may seem
a routine and yet, no forensic geneticist is exempt from dealing with challenging cases on …