Kline-felter syndrome - Revision history

Nnjm2: Some issues with the references.

2016-11-15T13:03:09Z

Some issues with the references.

← Older revision		Revision as of 13:03, 15 November 2016
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	Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[Male\|male]] [[Karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY~~. ~~<ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X [[Chromosome\|chromosome]] can either come from the [[Sperm cell\|sperm]] or the [[Egg cell\|egg]] during [[Fertilisation\|fertilisation]] or even added during the early stages of development~~. ~~<ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>		Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[Male\|male]] [[Karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY<ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref>. The extra X [[Chromosome\|chromosome]] can either come from the [[Sperm cell\|sperm]] or the [[Egg cell\|egg]] during [[Fertilisation\|fertilisation]] or even added during the early stages of development<ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>.

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common [[~~Sex_chromosome~~\|sex chromosome]] aneuploidy in males. The [[Phenotype\|phenotype]] of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common [[Sex chromosome\|sex chromosome]] aneuploidy in males. The [[Phenotype\|phenotype]] of the disorder is usually only presented after maturation.

	The most common symptoms of Kline-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.		The most common symptoms of Kline-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts<ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.

	=== References ===		=== References ===

	<references />		<references />

160183784 at 12:34, 15 November 2016

2016-11-15T12:34:05Z

← Older revision		Revision as of 12:34, 15 November 2016
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	Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[Male\|male]] [[Karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X [[Chromosome\|chromosome]] can either come from the [[Sperm cell\|sperm]] or the [[Egg cell\|egg]] during [[Fertilisation\|fertilisation]] or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>		Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[Male\|male]] [[Karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X [[Chromosome\|chromosome]] can either come from the [[Sperm cell\|sperm]] or the [[Egg cell\|egg]] during [[Fertilisation\|fertilisation]] or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common [[Sex_chromosome\|sex chromosome ]]aneuploidy in males. The [[Phenotype\|phenotype]] of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common [[Sex_chromosome\|sex chromosome]] aneuploidy in males. The [[Phenotype\|phenotype]] of the disorder is usually only presented after maturation.

	The most common symptoms of Kline-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.		The most common symptoms of Kline-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.

160183784 at 12:33, 15 November 2016

2016-11-15T12:33:25Z

← Older revision		Revision as of 12:33, 15 November 2016
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	Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[Male\|male]] [[Karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X [[Chromosome\|chromosome]] can either come from the [[~~Sperm_cell~~\|sperm]] or the [[~~egg~~ cell\|egg]] during [[~~fertilisation~~\|fertilisation]] or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>		Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[Male\|male]] [[Karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X [[Chromosome\|chromosome]] can either come from the [[Sperm cell\|sperm]] or the [[Egg cell\|egg]] during [[Fertilisation\|fertilisation]] or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The [[Phenotype\|phenotype]] of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common [[Sex_chromosome\|sex chromosome ]]aneuploidy in males. The [[Phenotype\|phenotype]] of the disorder is usually only presented after maturation.

	The most common symptoms of Kline-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.		The most common symptoms of Kline-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.

160183784: added links, fixed two spelling mistakes

2016-11-15T12:32:43Z

added links, fixed two spelling mistakes

← Older revision		Revision as of 12:32, 15 November 2016
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	Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[~~male~~\|male]] [[~~karyotype~~\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X chromosome can either come from the sperm or the egg during ~~fertlisation~~ or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>		Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[Male\|male]] [[Karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X [[Chromosome\|chromosome]] can either come from the [[Sperm_cell\|sperm]] or the [[egg cell\|egg]] during [[fertilisation\|fertilisation]] or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The [[~~phenotype~~\|phenotype]] of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The [[Phenotype\|phenotype]] of the disorder is usually only presented after maturation.

	The most common symptoms of ~~Kliene~~-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.		The most common symptoms of Kline-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.

	=== References ===		=== References ===

	<references />		<references />

Nnjm2 at 06:53, 26 November 2014

2014-11-26T06:53:37Z

← Older revision		Revision as of 06:53, 26 November 2014
Line 1:		Line 1:
	Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X chromosome can either come from the sperm or the egg during fertlisation or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>		Kline-felter syndrome is a genetic disorder found in males adding an extra [[X chromosme\|X chromosme]] to the normal [[male\|male]] [[karyotype\|karyotype]]. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X chromosome can either come from the sperm or the egg during fertlisation or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The [[phenotype\|phenotype]] of the disorder is usually only presented after maturation.

	The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.		The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.

140072244 at 21:25, 25 November 2014

2014-11-25T21:25:25Z

← Older revision		Revision as of 21:25, 25 November 2014
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	Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males.		Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males. In some cases the extra X chromosome is distrubuted unevenly throughout the body, this is refered to as mosaic Klinefelter syndrome. In even more rare cases the male with Klinefelter syndrome can have the karyotype 48, XXXY 48, XXYY or even 49, XXXXY. <ref>Mayo Clinic Staff (2013) Klinefelter syndrome, Mayo Clinic. Klinefelter syndrome Causes - Diseases and Conditions - Mayo Clinic. Available at: http://www.mayoclinic.org/diseases-conditions/klinefelter-syndrome/basics/causes/con-20033637 (Accessed: 25 November 2014).</ref> The extra X chromosome can either come from the sperm or the egg during fertlisation or even added during the early stages of development. <ref>Andrology Australia (2014) Klinefelter’s syndrome, Andrology Australia. Klinefelter’s syndrome. Available at: https://www.andrologyaustralia.org/reproductive-problems/klinefelters-syndrome/ (Accessed: 25 November 2014).</ref>

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.

	The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>.		The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>. Other symptoms can include delayed puberty, weak bones and a risk of certain cancers including breast and bone cancers.

	=== References ===		=== References ===

	<references />		<references />

Nnjm2: Wow, the last edit really broke the system. Cleaned up the material, removed the image, and removed the link to wikipedia.

2013-11-16T07:31:47Z

Wow, the last edit really broke the system. Cleaned up the material, removed the image, and removed the link to wikipedia.

← Older revision		Revision as of 07:31, 16 November 2013
Line 3:		Line 3:
	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.

	The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts~~.<ref>[(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]</ref>~~<ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones ~~&amp;amp;amp;~~ Bartlett Learning]</ref>		The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts <ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones and Bartlett Learning]</ref>.

	=== References ===		=== References ===

	<references />		<references />

Nnjm2 at 07:29, 16 November 2013

2013-11-16T07:29:45Z

← Older revision		Revision as of 07:29, 16 November 2013
Line 1:		Line 1:
	Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males.		Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males.

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.		This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.

	The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts.<ref>[(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]</ref><ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones &amp; Bartlett Learning]</ref>		The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts.<ref>[(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]</ref><ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones &amp;amp;amp; Bartlett Learning]</ref>

	~~[[Image:XXY karyotype]]~~		=== References ===

	~~References~~		<references />

	<references></~~references~~>

Nnjm2 at 07:28, 16 November 2013

2013-11-16T07:28:17Z

← Older revision		Revision as of 07:28, 16 November 2013
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	~~<u> Kliene-felter Syndrome</u>~~		Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males.

	~~<u></u> <u></u>~~ Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males.~~  <br>~~

	This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.  <br>

	~~The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts.<ref></ref>  <br>~~

			This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.

			The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts.<ref>[(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]</ref><ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones &amp; Bartlett Learning]</ref>

	[[Image:XXY karyotype]]		[[Image:XXY karyotype]]

			References

			<references></references>
	~~'''<u>References</u>'''~~ <references></references~~><br> <ref></ref> <ref></ref>~~

	~~<ref>[(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]</ref><br> <ref></ref> <ref></ref>~~

	~~<ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones &amp; Bartlett Learning]</ref~~>

130070944: Created page with " Kliene-felter Syndrome Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These in..."

2013-11-12T14:33:11Z

Created page with " Kliene-felter Syndrome Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These in..."

New page

Kliene-felter Syndrome

 Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males.  

This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.  

The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts.<ref></ref>  

[[Image:XXY karyotype]]

'''References''' <references></references> <ref></ref> <ref></ref>

<ref>[(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]</ref> <ref></ref> <ref></ref>

<ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones &amp; Bartlett Learning]</ref>