Clinical and genetic features of 45,X maleness: A case report and review of the literature.
- Author:
Qiu-Wen SHI
1
;
Chang-Long XU
1
;
Ni-Na LI
1
;
Wei LIU
1
;
Lan YANG
1
;
Li-Wen DENG
1
;
Ying QIU
1
Author Information
1. Center of Reproduction, Nanning Second People's Hospital, Nanning, Guangxi 530031, China.
- Publication Type:Case Reports
- Keywords:
45,X;
azoospermia;
karyotype;
maleness;
translocation
- MeSH:
Azoospermia;
genetics;
Chromosome Banding;
Chromosome Deletion;
Chromosomes, Human, Pair 14;
genetics;
Chromosomes, Human, Y;
genetics;
Gonadal Dysgenesis;
genetics;
Humans;
Infertility, Male;
genetics;
Karyotyping;
methods;
Male;
Polymerase Chain Reaction;
SOXB1 Transcription Factors;
genetics;
Translocation, Genetic;
genetics
- From:
National Journal of Andrology
2017;23(1):65-68
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To explore the relationship between the clinical and genetic features of a short-statured azoospermia male with the karyotype of 45,X.
METHODS:Using GTG-banded chromosome analysis, we performed karyotyping for a 150 cm-high infertile male with azoospermia and investigated the presence and location of the genes on the Y chromosome by FISH and PCR.
RESULTS:GTG-banded chromosome analysis showed the karyotype of the patient to be 45,X,add(14)(p11). The results of PCR manifested the deletion of AZFa, AZFb, AZFc, and AZFd in the SRY gene. FISH revealed the translocation of the short arm of the Y chromosome to that of chromosome 14 and deletion of most proportions of its long arm, with the disruption site close to the centromere region. The karyotype of the patient was 45,X,der(Y)t(Y;14)(q11;q11.2), 14.ish (SRY+, CEP Y+ , DYZ1－).
CONCLUSIONS:The karyotype of the patient was unbalanced Y/14 translocation. The SRY gene is the key to maleness. The deletion of AZFa－ d induces spermatogenic disturbance, and the deletion of the q arm of the Y chromosome may be related with short stature.
