COTS
Moss Bank
Manse Road
Lairg
IV27 4EL
Tel & Facsimile: 0844 414 0181 (local rate call) or 01549 402777
Calling from outside the UK 0044 1549 402777
Email:
robin@surrogacy.org.uk


T

Terminology Explanation                                             
Tay-Sachs is an inherited disease within the Jewish Community, and is carried in the parents' genetic make-up. If both parents are carriers of the Tay-Sachs gene the foetus has a 1 in 4 chance of developing the disease. The disease affects young children with destruction of the brain and nervous system leading to paralysis, blindness and fits. There is no cure for this condition.
Teratozoospermia Poor sperm morphology (shape) which cause infertility.
Testicular Sperm Aspiration (TESA) This sperm extraction technique involves the insertion of a needle into the lower region of the testes and the removal of a small piece of testicular tissue.
Testicular Sperm Extraction (TESE) This sperm extraction technique involves the exposure of testicular tissue through a small cut in the scrotum and the removal of a small piece of testicular tissue. Or, retrieving sperm directly from the testis.
Testis (plural - testes) Testicle or male gonad
Testosterone The male hormone responsible for the formation of secondary sex characteristics and for supporting the sex drive. Testosterone is also necessary for spermatogenesis (sperm development)
Test Tube Babies: The common name given to babies conceived outside the womb though IVF.
Traditional (Straight) surrogacy involves the surrogate using her own egg, fertilised by the intended father’s sperm by artificial insemination. It can be done in an IVF clinic or by the surrogate herself in the privacy of her own home.
Transvaginal aspiration: A method of egg recovery in which a needle is inserted through the top of the vagina into the ovary lining.
Treatment Cycle One complete licensed treatment. Commences with administration of drugs or first insemination.
Triplet or trinucleatide repeat disorders A range of genetic diseases caused by the expansion of a triplet repeat of bases within a gene and are usually associated with neurological disorders e.g. fragile X, Huntington disease, myotonic dystrophy. Each disease has a range of repeats associated with a spectrum from normal to affected individuals.
Trisomy A syndrome reflecting the presence of three chromosomes of one type instead of the normal human chromosome number of two. An example is Trisomy 21 resulting in Down's syndrome

 

 

 

 

 

 

 

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