Hypogonadotrophic short statured with anosmia: Kallmann's syndrome
Short stature with loss of secondary sex characters can occur due to genetic disorders. One of them is Kallmann's syndrome. The condition has been noted to be present in families. It is associated with anosmia and hypogonadism. We are presenting a case of young boy who was short statured and ha...
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| Veröffentlicht in: | Journal of the College of Physicians and Surgeons--Pakistan 2011-02, Vol.21 (2), p.113-114 |
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| container_title | Journal of the College of Physicians and Surgeons--Pakistan |
| container_volume | 21 |
| creator | Tarique, Shandana Iqbal, M Hassan Riaz, Hina Abaidullah, Sajid Cheema, Tahira Murtaza |
| description | Short stature with loss of secondary sex characters can occur due to genetic disorders. One of them is Kallmann's syndrome. The condition has been noted to be present in families. It is associated with anosmia and hypogonadism. We are presenting a case of young boy who was short statured and had anosmia with multiple hormonal deficiencies. |
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One of them is Kallmann's syndrome. The condition has been noted to be present in families. It is associated with anosmia and hypogonadism. 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One of them is Kallmann's syndrome. The condition has been noted to be present in families. It is associated with anosmia and hypogonadism. We are presenting a case of young boy who was short statured and had anosmia with multiple hormonal deficiencies.</description><subject>Adolescent</subject><subject>Diagnosis, Differential</subject><subject>Human Growth Hormone - therapeutic use</subject><subject>Humans</subject><subject>Kallmann Syndrome - diagnosis</subject><subject>Kallmann Syndrome - drug therapy</subject><subject>Male</subject><subject>Steroids - therapeutic use</subject><subject>Vitamin D - therapeutic use</subject><issn>1022-386X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j8FKxDAURbNQnHH0FyS7WRWS95q0daeDOuKAGwV35bVNbaVpapIi_XsHHDfnbg4XzhlbSwGQYK4_VuwyhC8hUMk8v2ArkIgIqV6z-_0yuU83UuOid1PX1zx0zkceIsXZm4b_9LHjNLpge7rlLzQMlsZxG3hYxsY7a67YeUtDMNen3bD3x4e33T45vD497-4OyQRSxAQkmQpFC6ogrEUrJSGlmRTCCEKkI3NdU6a1KjINSrVQNFWRZmkFoKDFDdv-_U7efc8mxNL2oTbDQKNxcyhzhWkmINNH8-ZkzpU1TTn53pJfyv9s_AUms1KT</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Tarique, Shandana</creator><creator>Iqbal, M Hassan</creator><creator>Riaz, Hina</creator><creator>Abaidullah, Sajid</creator><creator>Cheema, Tahira Murtaza</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201102</creationdate><title>Hypogonadotrophic short statured with anosmia: Kallmann's syndrome</title><author>Tarique, Shandana ; Iqbal, M Hassan ; Riaz, Hina ; Abaidullah, Sajid ; Cheema, Tahira Murtaza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p210t-21aeb30f259a3c0f11a3a47100e0a33ae0a86ca7665976255f29db9474b2252f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Diagnosis, Differential</topic><topic>Human Growth Hormone - therapeutic use</topic><topic>Humans</topic><topic>Kallmann Syndrome - diagnosis</topic><topic>Kallmann Syndrome - drug therapy</topic><topic>Male</topic><topic>Steroids - therapeutic use</topic><topic>Vitamin D - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tarique, Shandana</creatorcontrib><creatorcontrib>Iqbal, M Hassan</creatorcontrib><creatorcontrib>Riaz, Hina</creatorcontrib><creatorcontrib>Abaidullah, Sajid</creatorcontrib><creatorcontrib>Cheema, Tahira Murtaza</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the College of Physicians and Surgeons--Pakistan</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tarique, Shandana</au><au>Iqbal, M Hassan</au><au>Riaz, Hina</au><au>Abaidullah, Sajid</au><au>Cheema, Tahira Murtaza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypogonadotrophic short statured with anosmia: Kallmann's syndrome</atitle><jtitle>Journal of the College of Physicians and Surgeons--Pakistan</jtitle><addtitle>J Coll Physicians Surg Pak</addtitle><date>2011-02</date><risdate>2011</risdate><volume>21</volume><issue>2</issue><spage>113</spage><epage>114</epage><pages>113-114</pages><issn>1022-386X</issn><abstract>Short stature with loss of secondary sex characters can occur due to genetic disorders. One of them is Kallmann's syndrome. The condition has been noted to be present in families. It is associated with anosmia and hypogonadism. We are presenting a case of young boy who was short statured and had anosmia with multiple hormonal deficiencies.</abstract><cop>Pakistan</cop><pmid>21333246</pmid><tpages>2</tpages></addata></record> |
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| identifier | ISSN: 1022-386X |
| ispartof | Journal of the College of Physicians and Surgeons--Pakistan, 2011-02, Vol.21 (2), p.113-114 |
| issn | 1022-386X |
| language | eng |
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| source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
| subjects | Adolescent Diagnosis, Differential Human Growth Hormone - therapeutic use Humans Kallmann Syndrome - diagnosis Kallmann Syndrome - drug therapy Male Steroids - therapeutic use Vitamin D - therapeutic use |
| title | Hypogonadotrophic short statured with anosmia: Kallmann's syndrome |
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