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Skip to search form Skip to main content. Triple X syndrome. The Journal of the Pakistan Medical….

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Turner syndrome TSalso known 45,Xor 45,X0is a genetic condition in which a female is partly or completely missing an X chromosome. Turner syndrome is not usually inherited from a person's parents. No cure for Turner syndrome is known. Turner syndrome occurs in between one in 2, [6] and one in 5, females at birth.

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The developmental and clinical aspects in the literature on triple X syndrome are reviewed. Prenatal diagnosis depends on karyotyping. The incidence is 1 of females.

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At initial evaluation, reproductive and medical histories were collected. Clinical assessment of the child was performed by a clinical geneticist and included a detailed personal history, physical evaluation and auxological measurements. To analyse how parents coped with specific events in the prenatal and postnatal periods, we conducted an interview that included 35 specific questions designed to elicit retrospective judgements on prenatal communication, present and future worries, needs and expectations.

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Triple X syndromealso known as trisomy X and 47,XXXis characterized by the presence of an extra X chromosome in each cell of a female. Triple X is due to a random event. Treatment may include speech therapy, physical therapy, and counseling. Because the vast majority of triple X females are never diagnosed, it may be very difficult to make generalizations about the effects of this syndrome.

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