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Reproductive Endocrinology

Can Men With 47,XYY Syndrome Have Biological Children?

At a Glance

Yes, the vast majority of men with 47,XYY syndrome can have biological children and conceive naturally. While some may experience lower sperm counts, fertility treatments like IVF are highly successful, and it is very unlikely the condition will be passed on.

Yes, absolutely. The vast majority of men with 47,XYY syndrome are able to have biological children [1][2]. While a diagnosis of 47,XYY can naturally cause parents to worry about their child’s future, it is very common for men with this condition to conceive naturally when they are ready to start a family [2][3].

However, because 47,XYY can sometimes affect how sperm is produced, some men may experience fertility challenges that require medical support [4][5].

Natural Conception and Sperm Production

For many men with 47,XYY, sperm production is normal or sufficient enough to achieve pregnancy without any medical help [2][5].

For others, the extra Y chromosome can lead to oligozoospermia (a lower than average sperm count) or, less commonly, azoospermia (the absence of sperm in the semen) [1][6]. While some individuals may have variations in their hormonal profiles, hormone levels—including testosterone—are generally normal for most men with 47,XYY [1][7].

If a man with 47,XYY does have a low sperm count, it does not mean he cannot have biological children. Furthermore, unlike some other sex chromosome conditions (such as 47,XXY or Klinefelter syndrome), early fertility preservation—like freezing sperm during puberty—is generally not necessary for boys with 47,XYY.

Options for Fertility Support

When natural conception isn’t possible, Assisted Reproductive Technologies (ART) are highly successful for men with 47,XYY [5][6].

The most common approach is In Vitro Fertilization (IVF) combined with Intracytoplasmic Sperm Injection (ICSI) [5][8]. In this procedure, a single healthy sperm is isolated and directly injected into an egg [5]. Because ICSI requires very few sperm, it is an excellent option for men with low sperm counts [5]. In the rare event of azoospermia, minor procedures can often extract sperm directly from the testicles to be used in IVF [5].

Will He Pass the Extra Y Chromosome to His Children?

It is very unlikely that a man with 47,XYY will pass the condition to his children.

During the process of sperm creation, the body usually “corrects” the chromosome count. As a result, the vast majority of sperm produced by a man with 47,XYY have a typical chromosome count (either one X or one Y) [9][10].

However, studies show there is a very small number of sperm that may carry an extra sex chromosome [9][10]. Because of this, there is a slightly increased chance that an embryo could have a sex chromosome variation. Overall, only about 1.5% of embryos from men with 47,XYY have a sex chromosome difference, meaning that 98.5% of embryos have a typical chromosome count [5][11].

If your son eventually uses IVF to conceive, his doctors may recommend Preimplantation Genetic Testing (PGT) [12][8]. This involves screening the embryos for chromosomal differences before they are transferred to the uterus, ensuring that only embryos with a typical chromosome count are used [8]. Genetic counseling is generally recommended for adults with 47,XYY who are planning to start a family, especially if they are using fertility treatments [5][13].

Looking Ahead

Right now, your focus should be on your son’s healthy development. Fertility is not something that needs to be addressed or monitored during childhood or puberty. When your son reaches adulthood and decides he wants to have children, a simple semen analysis can tell him what his sperm count is and whether he might need to consult a fertility specialist.

Common questions in this guide

Do men with 47,XYY syndrome have normal sperm counts?
Many men with 47,XYY syndrome have normal sperm production and can conceive without medical help. However, some may experience a lower than average sperm count or, rarely, a complete absence of sperm in the semen.
Should boys with 47,XYY syndrome freeze their sperm?
No, early fertility preservation, such as freezing sperm during puberty, is generally not necessary for boys with 47,XYY syndrome. Fertility can simply be evaluated with a semen analysis once they reach adulthood and are ready to start a family.
Will a man with 47,XYY pass the condition to his children?
It is very unlikely. The body naturally corrects the chromosome count during sperm creation, which means that over 98% of embryos from men with 47,XYY have a typical chromosome count.
What fertility treatments are available for men with 47,XYY?
If natural conception is not possible due to low sperm count, Assisted Reproductive Technologies (ART) are highly successful. The most common approach is In Vitro Fertilization (IVF) combined with Intracytoplasmic Sperm Injection (ICSI).
What is Preimplantation Genetic Testing (PGT) and is it recommended?
Preimplantation Genetic Testing (PGT) is a screening process used during IVF. It allows doctors to check embryos for chromosomal differences before they are transferred to the uterus, ensuring only embryos with a typical chromosome count are used.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.When my son reaches adulthood, at what age should he consider getting a semen analysis if he wants to plan for a family?
  2. 2.Are there any physical signs during puberty that might indicate if his testicular development is progressing typically?
  3. 3.What is the best way to discuss his 47,XYY diagnosis with him as he grows up, so he understands his future fertility options without feeling anxious?
  4. 4.Can you connect us with a genetic counselor who can help us better understand the low risk of him passing on the condition?

Questions For You

Tap a prompt to share your answer — we'll use it plus this page's context to start a tailored conversation.

References

References (13)
  1. 1

    Gonadal function in patients with 47,XYY syndrome: a systematic review and meta-analysis.

    Cannarella R, Pedano A, Compagnone M, et al.

    Endocrine connections 2025; (14(4)).

    PMID: 39981656
  2. 2

    Clinical aspects of infertile 47,XYY patients: a retrospective study.

    Borjian Boroujeni P, Sabbaghian M, Vosough Dizaji A, et al.

    Human fertility (Cambridge, England) 2019; (22(2)):88-93 doi:10.1080/14647273.2017.1353143.

    PMID: 28715980
  3. 3

    Genetic investigations on causes of male infertility in Western Saudi Arabia.

    Beg MA, Nieschlag E, Abdel-Meguid TA, et al.

    Andrologia 2019; (51(6)):e13272 doi:10.1111/and.13272.

    PMID: 30907014
  4. 4

    High frequency of de novo DAZ microdeletion in sperm nuclei of subfertile men: possible involvement of genome instability in idiopathic male infertility.

    Mozdarani H, Ghoraeian P, Mozdarani S, et al.

    Human fertility (Cambridge, England) 2018; (21(2)):137-145 doi:10.1080/14647273.2017.1322718.

    PMID: 28521575
  5. 5

    Reproductive outcomes of 3 infertile males with XYY syndrome: Retrospective case series and literature review.

    Zhang X, Liu X, Xi Q, et al.

    Medicine 2020; (99(9)):e19375 doi:10.1097/MD.0000000000019375.

    PMID: 32118782
  6. 6

    Pituitary hyperplasia with Sertoli cell-only and 47,XYY syndromes: an uncommon triad.

    Ra AG, Evans PJ, Awasthi A, Srinivas-Shankar U

    BMJ case reports 2020; (13(5)) doi:10.1136/bcr-2019-233100.

    PMID: 32414773
  7. 7

    Fertility achieved through in vitro fertilization in a male patient with 48,XXYY syndrome.

    Liu DF, Zhao LM, Hong K, et al.

    Asian journal of andrology 2018; (20(2)):208-209 doi:10.4103/aja.aja_44_17.

    PMID: 28980534
  8. 8

    Outcomes of Preimplantation Genetic Diagnosis Cycles by Fluorescent In situ Hybridization of Infertile Males with Nonmosaic 47,XYY Syndrome.

    Xu C, Zhang FF, Li HC, et al.

    Chinese medical journal 2018; (131(15)):1808-1812 doi:10.4103/0366-6999.237393.

    PMID: 30058577
  9. 9

    Selective advantage of euploid spermatocytes I in an azoospermic 47,XYY man with gonadal mosaicism.

    Sciurano RB, Rahn IM, González Arias B, et al.

    Human reproduction (Oxford, England) 2019; (34(3)):568-573 doi:10.1093/humrep/dey387.

    PMID: 30597018
  10. 10

    Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia.

    Wu C, Wang L, Iqbal F, et al.

    Molecular cytogenetics 2016; (9()):9 doi:10.1186/s13039-016-0218-z.

    PMID: 26839593
  11. 11

    Preimplantation genetic testing might not be the necessity for male patients with 47,XYY syndrome: A pilot study.

    Dong F, Zheng Z, Ding Y, et al.

    Reproductive medicine and biology 2025; (24(1)):e12650 doi:10.1002/rmb2.12650.

    PMID: 40264980
  12. 12

    Use of suboptimal sperm increases the risk of aneuploidy of the sex chromosomes in preimplantation blastocyst embryos.

    Coates A, Hesla JS, Hurliman A, et al.

    Fertility and sterility 2015; (104(4)):866-872 doi:10.1016/j.fertnstert.2015.06.033.

    PMID: 26183314
  13. 13

    Health professionals' involvement and information provision in genetic counseling following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong.

    So PL, Cheng YKY, Cheuk KY, et al.

    International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2019; (144(3)):314-316 doi:10.1002/ijgo.12737.

    PMID: 30516269

This page provides educational information about fertility and 47,XYY syndrome. It is not a substitute for professional medical advice; always consult a fertility specialist or genetic counselor regarding your specific situation.

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