45,X/46,XY Mosaicism - Wikipedia

Medical condition

45,X/46,XY mosaicism
Other names	45,X0/46,XY MGD
Specialty	Obstetrics and gynaecology, endocrinology, medical genetics

45,X/46,XY mosaicism, also known as X0/XY mosaicism and mixed gonadal dysgenesis,[1] is a mutation of sex development in humans associated with sex chromosome aneuploidy and mosaicism of the Y chromosome. It is a fairly rare chromosomal disorder at birth, with an estimated incidence rate of about 1 in 15,000 live births.[2] Mosaic loss of the Y chromosome in previously non-mosaic men grows increasingly common with age.[3]

The clinical manifestations are highly variable, ranging from partial virilisation and ambiguous genitalia at birth, to patients with completely male or female gonads. Most individuals with this karyotype have apparently normal male genitalia, and a minority have female genitalia, with a significant number of individuals showing genital abnormalities or mixed sex characteristics.[4] A significantly higher than average number of other developmental abnormalities are also found in individuals with X0/XY mosaicism.[4] Psychomotor development is normal.

Signs and symptoms

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Conditions can be distinguished histologically and by karyotyping.[5] The observable characteristics (phenotype) of this condition are highly variable, ranging from gonadal dysgenesis in males, to Turner-like females and phenotypically normal males.[6] The phenotypical expression may be ambiguous, male or female, regardless of the extent of the mosaicism.[7] The most common presentation of 45,X/46,XY karyotype is phenotypically normal male, next being genital ambiguity.[8]

There is a range of chromosomal anomalies within 45,X/46,XY where the variations are very complex, and the actual result in living individuals is often not a simple picture.[1] Most patients with this karyotype are known to have abnormal gonadal histology and heights considerably below their genetic potential. High gonadotropin levels have been described in both male and female patients, as well as low levels of testosterone in male patients. Dosage loss of SHOX gene is commonly associated with short stature.[9] Psychomotor development is normal.[citation needed]

As the gonads may not be symmetrical, the development of the Müllerian duct and Wolffian duct may be asymmetrical, too.[10] Because of the presence of dysgenetic gonadal tissue and Y chromosome material, there is a high risk of the development of a gonadoblastoma.[1]

Causes

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In a normal situation, all the cells in an individual will have 46 chromosomes, with one being an X and one a Y or with two Xs. However, sometimes during the early copying processes of DNA replication and cell division, one chromosome can be lost. In 45,X/46,XY, most or all of the Y chromosome is lost in one of the newly created cells. All the cells then made from this cell will lack the Y chromosome. All the cells created from the cells that have not lost the Y chromosome will be XY.[11] The 46,XY cells will continue to multiply at the same time as the 45,X cells multiply. The embryo, then the fetus, and then eventually the baby will have what is known as a 45,X/46,XY constitution.

There are many chromosomal variations that cause the 45,X/46,XY karyotype, including malformation (isodicentricism) of the Y chromosomes, deletions of Y chromosome or translocations of Y chromosome segments.[2] Such rearrangements of the Y chromosome can lead to partial expression of the SRY gene which may lead to abnormal genitals and testosterone levels.[citation needed][original research?]

Diagnosis

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Identification of 45,X/46,XY karyotype has significant clinical implications due to known effects on growth, hormonal balance, gonadal development and histology.[2] 45,X/46,XY is diagnosed by examining the chromosomes in a blood sample.

The age of diagnosis varies depending on manifestations of disease prompting reason for cytogenetic testing. Many patients are diagnosed prenatally due to fetal factors (increased nuchal fold, or abnormal levels of serum), maternal age or abnormal ultrasounds, while others will be diagnosed postnatal due to external genital malformation.[2] It is not uncommon for patients to be diagnosed later in life due to short stature or delayed puberty, or a combination of both.[8]

45,X/46,XY mosaicism can be detected prenatally through amniocentesis however, it was determined that the proportion of 45,X cells in the amniotic fluid cannot predict any phenotypic outcomes, often making prenatal genetic counselling difficult.[6]

Management

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See also

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• Sex chromosome anomalies
• Gonadal dysgenesis
• Mosaic (genetics)
• Turner syndrome

References

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1. ^ a b c "45,X/46,XY including Y chromosome rearrangements" (PDF). rarechromo.org. Retrieved 15 July 2024.
2. ^ a b c d Johansen, Marie Lindhart; et al. (1 August 2012). "45,X/46,XY Mosaicism: Phenotypic Characteristics, Growth, and Reproductive Function—A Retrospective Longitudinal Study". The Journal of Clinical Endocrinology & Metabolism. 97 (8): E1540–E1549. doi:10.1210/jc.2012-1388. PMID 22605431.
3. ^ Zhou W, Machiela MJ, Freedman ND, Rothman N, Malats N, Dagnall C, et al. (2016). "Mosaic loss of chromosome Y is associated with common variation near TCL1A". Nat Genet. 48 (5): 563–8. doi:10.1038/ng.3545. PMC 4848121. PMID 27064253.
4. ^ a b Chang, H. J.; Clark, R. D.; Bachman, H. (1990). "The phenotype of 45,X/46,XY mosaicism: An analysis of 92 prenatally diagnosed cases". American Journal of Human Genetics. 46 (1): 156–167. PMC 1683543. PMID 2294747.
5. ^ Kim KR, Kwon Y, Joung JY, Kim KS, Ayala AG, Ro JY (October 2002). "True hermaphroditism and mixed gonadal dysgenesis in young children: a clinicopathologic study of 10 cases". Mod. Pathol. 15 (10): 1013–9. doi:10.1097/01.MP.0000027623.23885.0D. PMID 12379746.
6. ^ a b Hsu LY (January 1989). "Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update". Prenat. Diagn. 9 (1): 31–48. doi:10.1002/pd.1970090106. PMID 2664755. S2CID 20193032.
7. ^ Chang, H J; et al. (1990). "The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases". American Journal of Human Genetics. 46 (1): 156–167. PMC 1683543. PMID 2294747.
8. ^ a b Efthymiadou A, Stefanou EG, Chrysis D (2012). "45,X/46,XY mosaicism: a cause of short stature in males". Hormones (Athens). 11 (4): 501–4. doi:10.14310/horm.2002.1384. PMID 23422775.
9. ^ 45,X/46,XY mixed gonadal dysgenesis Archived 2017-04-17 at the Wayback Machine. Orfa.net; August 2015.
10. ^ Donahoe PK, Crawford JD, Hendren WH (1979). "Mixed gonadal dysgenesis, pathogenesis, and management". J. Pediatr. Surg. 14 (3): 287–300. doi:10.1016/S0022-3468(79)80486-8. PMID 480090.
11. ^ 45,X/46,XY Mosaicism: Report of 27 Cases Archived 2019-12-16 at the Wayback Machine. Pediatrics Vol. 104 No. 2 August 1, 1999. pp. 304 -308

External links

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Classification	D ICD-10: Q96.3 ICD-9-CM: 758.6 MeSH: D006060 DiseasesDB: 29266
External resources	Orphanet: 1772

v t e Female and male congenital anomalies of the genitalia, including intersex and DSD
Internal	Uterine malformation Müllerian agenesis Cervical agenesis Unicornuate uterus Uterus didelphys Bicornuate uterus Uterine septum Arcuate uterus Vagina Vaginal septum Vaginal hypoplasia Imperforate hymen Vaginal adenosis Cloacal exstrophy Vaginal atresia Gonads Testicle Cryptorchidism Polyorchidism Monorchism Sertoli cell-only syndrome Ovary XX gonadal dysgenesis Unilateral ovarian agenesis Other Gonadal agenesis Ovotesticular syndrome Mixed gonadal dysgenesis XY gonadal dysgenesis Vas deferens Congenital absence of the vas deferens Other Persistent Müllerian duct syndrome
External	Penis Hypospadias Epispadias Chordee Micropenis Aphallia Diphallia Penoscrotal transposition Other Clitoromegaly Progestin-induced virilization Pseudohermaphroditism True hermaphroditism

v t e Chromosome abnormalities
Autosomal	Duplications,including trisomies 1q21.1 duplication syndrome 2q31.1 microduplication Trisomy 8 Trisomy 9 Tetrasomy 9p Distal trisomy 10q Patau syndrome 13 Trisomy 16 16p11.2 duplication syndrome Trisomy 18 Down syndrome 21 22q11.2 duplication syndrome Trisomy 22 Cat-eye syndrome 22 Deletions (1q21.1 copy number variations/1q21.1 deletion syndrome/1q21.1 duplication syndrome/TAR syndrome/1p36 deletion syndrome) 1 Wolf–Hirschhorn syndrome 4 Cri du chat syndrome/Chromosome 5q deletion syndrome 5 Williams syndrome 7 Jacobsen syndrome 11 Miller–Dieker syndrome/Smith–Magenis syndrome/17q12 microdeletion syndrome 17 DiGeorge syndrome 22 22q11.2 distal deletion syndrome 22 22q13 deletion syndrome 22 genomic imprinting Angelman syndrome/Prader–Willi syndrome (15) Distal 18q-/Proximal 18q-
X/Y linked	Monosomies Turner syndrome (45,X) Trisomies/tetrasomies,other karyotypes/mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48,XXXY) XXXYY syndrome (49,XXXYY) XXXXY syndrome (49,XXXXY) Trisomy X (47,XXX) Tetrasomy X (48,XXXX) Pentasomy X (49,XXXXX) XYY syndrome (47,XYY) XYYY syndrome (48,XYYY) XYYYY syndrome (49,XYYYY) 45,X/46,XY 46,XX/46,XY
Translocations	Leukemia/lymphoma Lymphoid Burkitt lymphoma t(8 MYC;14 IGH) Follicular lymphoma t(14 IGH;18 BCL2) Mantle cell lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22 BCR) Acute myeloblastic leukemia with maturation t(8 RUNX1T1;21 RUNX1) Acute promyelocytic leukemia t(15 PML,17 RARA) Acute megakaryoblastic leukemia t(1 RBM15;22 MKL1) Other Ewing sarcoma t(11 FLI1; 22 EWS) Synovial sarcoma t(x SYT;18 SSX) Dermatofibrosarcoma protuberans t(17 COL1A1;22 PDGFB) Myxoid liposarcoma t(12 DDIT3; 16 FUS) Desmoplastic small-round-cell tumor t(11 WT1; 22 EWS) Alveolar rhabdomyosarcoma t(2 PAX3; 13 FOXO1) t (1 PAX7; 13 FOXO1)
Other	Fragile X syndrome Uniparental disomy XX male syndrome/46,XX testicular disorders of sex development Marker chromosome Ring chromosome 6; 9; 14; 15; 18; 20; 21, 22

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