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<meta name="keywords" content="C1854540, carney complex type 2, carney complex, type 2, carney complex, type ii, carney myxoma endocrine complex, type ii, carney myxoma-endocrine complex, type 2, carney myxoma-endocrine complex, type ii, cnc2, disease or syndrome, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="Carney complex (CNC) is characterized by skin pigmentary abnormalities, myxomas, endocrine tumors or overactivity, and schwannomas. Pale brown to black lentigines are the most common presenting feature of CNC and typically increase in number at puberty. Cardiac myxomas occur at a young age, may occur in any or all cardiac chambers, and can manifest as intracardiac obstruction of blood flow, embolic phenomenon, and/or heart failure. Other sites for myxomas include the skin, breast, oropharynx, and female genital tract. Primary pigmented nodular adrenocortical disease (PPNAD), which causes Cushing syndrome, is the most frequently observed endocrine tumor in CNC, occurring in approximately 25% of affected individuals. Large cell calcifying Sertoli cell tumors (LCCSCTs) are observed in one third of affected males within the first decade and in most adult males. Up to 75% of individuals with CNC have multiple thyroid nodules, most of which are nonfunctioning thyroid follicular adenomas. Clinically evident acromegaly from a growth hormone (GH)-producing adenoma is evident in approximately 10% of adults. Psammomatous melanotic schwannoma (PMS), a rare tumor of the nerve sheath, occurs in an estimated 10% of affected individuals. The median age of diagnosis is 20 years." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=340253
|
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ConceptID=C1854540
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Carney complex type 2<span class="h1sub">(CNC2)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>340253</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1854540</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>CARNEY MYXOMA-ENDOCRINE COMPLEX, TYPE 2</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0011525" target="_blank">MONDO:0011525</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/605244" target="_blank">605244</a></td></tr>
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</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_101">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Disease_characteristics">Disease characteristics</h1><a sid="101" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><div class="excerpt">Excerpted from the <i>GeneReview: </i><a href="/books/NBK1286" target="_blank">Carney Complex</a></div><div>Carney complex (CNC) is characterized by skin pigmentary abnormalities, myxomas, endocrine tumors or overactivity, and schwannomas. Pale brown to black lentigines are the most common presenting feature of CNC and typically increase in number at puberty. Cardiac myxomas occur at a young age, may occur in any or all cardiac chambers, and can manifest as intracardiac obstruction of blood flow, embolic phenomenon, and/or heart failure. Other sites for myxomas include the skin, breast, oropharynx, and female genital tract. Primary pigmented nodular adrenocortical disease (PPNAD), which causes Cushing syndrome, is the most frequently observed endocrine tumor in CNC, occurring in approximately 25% of affected individuals. Large cell calcifying Sertoli cell tumors (LCCSCTs) are observed in one third of affected males within the first decade and in most adult males. Up to 75% of individuals with CNC have multiple thyroid nodules, most of which are nonfunctioning thyroid follicular adenomas. Clinically evident acromegaly from a growth hormone (GH)-producing adenoma is evident in approximately 10% of adults. Psammomatous melanotic schwannoma (PMS), a rare tumor of the nerve sheath, occurs in an estimated 10% of affected individuals. The median age of diagnosis is 20 years. [from <a title="GeneReviews" href="https://www.ncbi.nlm.nih.gov/books/NBK1116" class="defSource" target="_blank">GeneReviews</a>]</div><div class="spaceAbove"><strong>Full text of <i>GeneReview</i> (by section):</strong><br /><a class="medgenPMinfo" href="/books/NBK1286#carney.Summary" target="NBK1286">Summary</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Diagnosis" target="NBK1286">Diagnosis</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Clinical_Characteristics" target="NBK1286">Clinical Characteristics</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Genetically_Related_Allelic_Disor" target="NBK1286">Genetically Related (Allelic) Disorders</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Differential_Diagnosis" target="NBK1286">Differential Diagnosis</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Management" target="NBK1286">Management</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Genetic_Counseling" target="NBK1286">Genetic Counseling</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Resources" target="NBK1286">Resources</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Molecular_Genetics" target="NBK1286">Molecular Genetics</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.Chapter_Notes" target="NBK1286">Chapter Notes</a> | <a class="medgenPMinfo" href="/books/NBK1286#carney.References" target="NBK1286">References</a></div><div class="spaceAbove"><strong>Authors:</strong><br />
|
||
Constantine A Stratakis <a href="/books/NBK1286" target="NBK1286" title="NCBI Bookshelf: Carney Complex">view full author information</a></div></div>
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<div class="portlet mgSection" id="ID_117">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Additional_description">Additional description</h1><a sid="117" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><div class="mgSection"><strong>From MedlinePlus Genetics</strong><br />Almost all people with Carney complex have areas of unusual skin pigmentation. Brown skin spots called lentigines may appear anywhere on the body but tend to occur around the lips, eyes, or genitalia. In addition, some affected individuals have at least one blue-black mole called a blue nevus.<br /><br />Some people with Carney complex develop a rare tumor called psammomatous melanotic schwannoma. This tumor occurs in specialized cells called Schwann cells, which wrap around and insulate nerves. This tumor is usually benign, but in some cases it can become cancerous (malignant).<br /><br />People with Carney complex may also develop tumors of other endocrine tissues, including the thyroid, testes, and ovaries. A tumor called an adenoma may form in the pituitary gland, which is located at the base of the brain. A pituitary adenoma usually results in the production of too much growth hormone. Excess growth hormone leads to acromegaly, a condition characterized by large hands and feet, arthritis, and "coarse" facial features.<br /><br />Individuals with Carney complex also develop tumors in hormone-producing (endocrine) glands, such as the adrenal glands located on top of each kidney. People with this condition may develop a specific type of adrenal disease called primary pigmented nodular adrenocortical disease (PPNAD). PPNAD causes the adrenal glands to produce an excess of the hormone cortisol. High levels of cortisol (hypercortisolism) can lead to the development of Cushing syndrome. This syndrome causes weight gain in the face and upper body, slowed growth in children, fragile skin, fatigue, and other health problems.<br /><br />Individuals with Carney complex are at increased risk of developing noncancerous (benign) tumors called myxomas in the heart (cardiac myxoma) and other parts of the body. Cardiac myxomas may be found in any of the four chambers of the heart and can develop in more than one chamber. These tumors can block the flow of blood through the heart, causing serious complications or sudden death. Myxomas may also develop on the skin and in internal organs. Skin myxomas appear as small bumps on the surface of the skin or as lumps underneath the skin. In Carney complex, myxomas have a tendency to recur after they are removed.<br /><br />Carney complex is a disorder characterized by an increased risk of several types of tumors. Affected individuals also usually have changes in skin coloring (pigmentation). Signs and symptoms of this condition commonly begin in the teens or early adulthood. <a target="_blank" href="https://medlineplus.gov/genetics/condition/carney-complex">https://medlineplus.gov/genetics/condition/carney-complex</a></div></div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0406810[DISCUI]&test_type=Clinical" ref="ncbi_uid=140810">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=140810" target="_blank" href="/omim/160980">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1286/" ref="ncbi_uid=140810">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=140810" ref="ncbi_uid=140810">V</a></span></span><span class="TLline"><a href="/medgen/140810" ref="tree=GTR&ncbi_uid=140810&link_uid=140810" title="View MedGen record for 'Carney complex'">Carney complex</a></span><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=340253" target="_blank" href="/omim/605244">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1286/" ref="ncbi_uid=340253">G</a></span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Carney complex type 2</span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C2607929[DISCUI]&test_type=Clinical" ref="ncbi_uid=388559">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=388559" target="_blank" href="/omim/160980">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1286/" ref="ncbi_uid=388559">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=388559" ref="ncbi_uid=388559">V</a></span></span><span class="TLline"><a href="/medgen/388559" ref="tree=GTR&ncbi_uid=388559&link_uid=388559" title="View MedGen record for 'Carney complex, type 1'">Carney complex, type 1</a></span></li></ul></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/11449" ref="tree=MeSH" title="MedGen record for Congenital anomaly of skin">Congenital anomaly of skin</a></span><ul><li><span class="TLline"><a href="/medgen/140810" ref="tree=MeSH" title="MedGen record for Carney complex">Carney complex</a></span><ul><li><span class="matched_ds">Carney complex type 2</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38007383">Genetic Testing in Hereditary Pituitary Tumors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Akkuş G,
|
||
Korbonits M</span><br />
|
||
<span class="medgenPMjournal">Arch Med Res</span>
|
||
2023 Dec;54(8):102920.
|
||
Epub 2023 Nov 24
|
||
doi: 10.1016/j.arcmed.2023.102920.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38007383" target="_blank">38007383</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37109772">Pituitary Tumorigenesis-Implications for Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vamvoukaki R,
|
||
Chrysoulaki M,
|
||
Betsi G,
|
||
Xekouki P</span><br />
|
||
<span class="medgenPMjournal">Medicina (Kaunas)</span>
|
||
2023 Apr 21;59(4)
|
||
doi: 10.3390/medicina59040812.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37109772" target="_blank">37109772</a><a href="/pmc/articles/PMC10145673" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35349723">Molecular genetic testing in the management of pituitary disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Coopmans EC,
|
||
Korbonits M</span><br />
|
||
<span class="medgenPMjournal">Clin Endocrinol (Oxf)</span>
|
||
2022 Oct;97(4):424-435.
|
||
Epub 2022 Mar 29
|
||
doi: 10.1111/cen.14706.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35349723" target="_blank">35349723</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(carney%20complex%20type%202)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (43)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35379992">New insights into the genetic etiology of Alzheimer's disease and related dementias.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bellenguez C,
|
||
Küçükali F,
|
||
Jansen IE,
|
||
Kleineidam L,
|
||
Moreno-Grau S,
|
||
Amin N,
|
||
Naj AC,
|
||
Campos-Martin R,
|
||
Grenier-Boley B,
|
||
Andrade V,
|
||
Holmans PA,
|
||
Boland A,
|
||
Damotte V,
|
||
van der Lee SJ,
|
||
Costa MR,
|
||
Kuulasmaa T,
|
||
Yang Q,
|
||
de Rojas I,
|
||
Bis JC,
|
||
Yaqub A,
|
||
Prokic I,
|
||
Chapuis J,
|
||
Ahmad S,
|
||
Giedraitis V,
|
||
Aarsland D,
|
||
Garcia-Gonzalez P,
|
||
Abdelnour C,
|
||
Alarcón-Martín E,
|
||
Alcolea D,
|
||
Alegret M,
|
||
Alvarez I,
|
||
Álvarez V,
|
||
Armstrong NJ,
|
||
Tsolaki A,
|
||
Antúnez C,
|
||
Appollonio I,
|
||
Arcaro M,
|
||
Archetti S,
|
||
Pastor AA,
|
||
Arosio B,
|
||
Athanasiu L,
|
||
Bailly H,
|
||
Banaj N,
|
||
Baquero M,
|
||
Barral S,
|
||
Beiser A,
|
||
Pastor AB,
|
||
Below JE,
|
||
Benchek P,
|
||
Benussi L,
|
||
Berr C,
|
||
Besse C,
|
||
Bessi V,
|
||
Binetti G,
|
||
Bizarro A,
|
||
Blesa R,
|
||
Boada M,
|
||
Boerwinkle E,
|
||
Borroni B,
|
||
Boschi S,
|
||
Bossù P,
|
||
Bråthen G,
|
||
Bressler J,
|
||
Bresner C,
|
||
Brodaty H,
|
||
Brookes KJ,
|
||
Brusco LI,
|
||
Buiza-Rueda D,
|
||
Bûrger K,
|
||
Burholt V,
|
||
Bush WS,
|
||
Calero M,
|
||
Cantwell LB,
|
||
Chene G,
|
||
Chung J,
|
||
Cuccaro ML,
|
||
Carracedo Á,
|
||
Cecchetti R,
|
||
Cervera-Carles L,
|
||
Charbonnier C,
|
||
Chen HH,
|
||
Chillotti C,
|
||
Ciccone S,
|
||
Claassen JAHR,
|
||
Clark C,
|
||
Conti E,
|
||
Corma-Gómez A,
|
||
Costantini E,
|
||
Custodero C,
|
||
Daian D,
|
||
Dalmasso MC,
|
||
Daniele A,
|
||
Dardiotis E,
|
||
Dartigues JF,
|
||
de Deyn PP,
|
||
de Paiva Lopes K,
|
||
de Witte LD,
|
||
Debette S,
|
||
Deckert J,
|
||
Del Ser T,
|
||
Denning N,
|
||
DeStefano A,
|
||
Dichgans M,
|
||
Diehl-Schmid J,
|
||
Diez-Fairen M,
|
||
Rossi PD,
|
||
Djurovic S,
|
||
Duron E,
|
||
Düzel E,
|
||
Dufouil C,
|
||
Eiriksdottir G,
|
||
Engelborghs S,
|
||
Escott-Price V,
|
||
Espinosa A,
|
||
Ewers M,
|
||
Faber KM,
|
||
Fabrizio T,
|
||
Nielsen SF,
|
||
Fardo DW,
|
||
Farotti L,
|
||
Fenoglio C,
|
||
Fernández-Fuertes M,
|
||
Ferrari R,
|
||
Ferreira CB,
|
||
Ferri E,
|
||
Fin B,
|
||
Fischer P,
|
||
Fladby T,
|
||
Fließbach K,
|
||
Fongang B,
|
||
Fornage M,
|
||
Fortea J,
|
||
Foroud TM,
|
||
Fostinelli S,
|
||
Fox NC,
|
||
Franco-Macías E,
|
||
Bullido MJ,
|
||
Frank-García A,
|
||
Froelich L,
|
||
Fulton-Howard B,
|
||
Galimberti D,
|
||
García-Alberca JM,
|
||
García-González P,
|
||
Garcia-Madrona S,
|
||
Garcia-Ribas G,
|
||
Ghidoni R,
|
||
Giegling I,
|
||
Giorgio G,
|
||
Goate AM,
|
||
Goldhardt O,
|
||
Gomez-Fonseca D,
|
||
González-Pérez A,
|
||
Graff C,
|
||
Grande G,
|
||
Green E,
|
||
Grimmer T,
|
||
Grünblatt E,
|
||
Grunin M,
|
||
Gudnason V,
|
||
Guetta-Baranes T,
|
||
Haapasalo A,
|
||
Hadjigeorgiou G,
|
||
Haines JL,
|
||
Hamilton-Nelson KL,
|
||
Hampel H,
|
||
Hanon O,
|
||
Hardy J,
|
||
Hartmann AM,
|
||
Hausner L,
|
||
Harwood J,
|
||
Heilmann-Heimbach S,
|
||
Helisalmi S,
|
||
Heneka MT,
|
||
Hernández I,
|
||
Herrmann MJ,
|
||
Hoffmann P,
|
||
Holmes C,
|
||
Holstege H,
|
||
Vilas RH,
|
||
Hulsman M,
|
||
Humphrey J,
|
||
Biessels GJ,
|
||
Jian X,
|
||
Johansson C,
|
||
Jun GR,
|
||
Kastumata Y,
|
||
Kauwe J,
|
||
Kehoe PG,
|
||
Kilander L,
|
||
Ståhlbom AK,
|
||
Kivipelto M,
|
||
Koivisto A,
|
||
Kornhuber J,
|
||
Kosmidis MH,
|
||
Kukull WA,
|
||
Kuksa PP,
|
||
Kunkle BW,
|
||
Kuzma AB,
|
||
Lage C,
|
||
Laukka EJ,
|
||
Launer L,
|
||
Lauria A,
|
||
Lee CY,
|
||
Lehtisalo J,
|
||
Lerch O,
|
||
Lleó A,
|
||
Longstreth W Jr,
|
||
Lopez O,
|
||
de Munain AL,
|
||
Love S,
|
||
Löwemark M,
|
||
Luckcuck L,
|
||
Lunetta KL,
|
||
Ma Y,
|
||
Macías J,
|
||
MacLeod CA,
|
||
Maier W,
|
||
Mangialasche F,
|
||
Spallazzi M,
|
||
Marquié M,
|
||
Marshall R,
|
||
Martin ER,
|
||
Montes AM,
|
||
Rodríguez CM,
|
||
Masullo C,
|
||
Mayeux R,
|
||
Mead S,
|
||
Mecocci P,
|
||
Medina M,
|
||
Meggy A,
|
||
Mehrabian S,
|
||
Mendoza S,
|
||
Menéndez-González M,
|
||
Mir P,
|
||
Moebus S,
|
||
Mol M,
|
||
Molina-Porcel L,
|
||
Montrreal L,
|
||
Morelli L,
|
||
Moreno F,
|
||
Morgan K,
|
||
Mosley T,
|
||
Nöthen MM,
|
||
Muchnik C,
|
||
Mukherjee S,
|
||
Nacmias B,
|
||
Ngandu T,
|
||
Nicolas G,
|
||
Nordestgaard BG,
|
||
Olaso R,
|
||
Orellana A,
|
||
Orsini M,
|
||
Ortega G,
|
||
Padovani A,
|
||
Paolo C,
|
||
Papenberg G,
|
||
Parnetti L,
|
||
Pasquier F,
|
||
Pastor P,
|
||
Peloso G,
|
||
Pérez-Cordón A,
|
||
Pérez-Tur J,
|
||
Pericard P,
|
||
Peters O,
|
||
Pijnenburg YAL,
|
||
Pineda JA,
|
||
Piñol-Ripoll G,
|
||
Pisanu C,
|
||
Polak T,
|
||
Popp J,
|
||
Posthuma D,
|
||
Priller J,
|
||
Puerta R,
|
||
Quenez O,
|
||
Quintela I,
|
||
Thomassen JQ,
|
||
Rábano A,
|
||
Rainero I,
|
||
Rajabli F,
|
||
Ramakers I,
|
||
Real LM,
|
||
Reinders MJT,
|
||
Reitz C,
|
||
Reyes-Dumeyer D,
|
||
Ridge P,
|
||
Riedel-Heller S,
|
||
Riederer P,
|
||
Roberto N,
|
||
Rodriguez-Rodriguez E,
|
||
Rongve A,
|
||
Allende IR,
|
||
Rosende-Roca M,
|
||
Royo JL,
|
||
Rubino E,
|
||
Rujescu D,
|
||
Sáez ME,
|
||
Sakka P,
|
||
Saltvedt I,
|
||
Sanabria Á,
|
||
Sánchez-Arjona MB,
|
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GR@ACE;
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DEGESCO;
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EADI;
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GERAD;
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Demgene;
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FinnGen;
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ADGC;
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Zulaica M;
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EADB;
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GR@ACE;
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DEGESCO;
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EADI;
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GERAD;
|
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Demgene;
|
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FinnGen;
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ADGC;
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CHARGE,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Carney%20complex%20type%202%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (76)</a></div><h3 class="subhead">Prognosis</h3>
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Windle G,
|
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Woods B,
|
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Yannakoulia M,
|
||
Zare H,
|
||
Zhao Y,
|
||
Zhang X,
|
||
Zhu C,
|
||
Zulaica M;
|
||
EADB;
|
||
GR@ACE;
|
||
DEGESCO;
|
||
EADI;
|
||
GERAD;
|
||
Demgene;
|
||
FinnGen;
|
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ADGC;
|
||
CHARGE,
|
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Farrer LA,
|
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Psaty BM,
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Ghanbari M,
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Raj T,
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Sachdev P,
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Jessen F,
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Amouyel P,
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Williams J,
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Frikke-Schmidt R,
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Clarimon J,
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Deleuze JF,
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Rossi G,
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Andreassen OA,
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<div class="nl"><a target="_blank" href="/pubmed/31169996">Succinate Dehydrogenase-Deficient Gastrointestinal Stromal Tumors.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/35379992">New insights into the genetic etiology of Alzheimer's disease and related dementias.</a></div>
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GR@ACE;
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Demgene;
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Epub 2022 Apr 4
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<span class="bold">PMID: </span><a href="/pubmed/35379992" target="_blank">35379992</a><a href="/pmc/articles/PMC9005347" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34583876">The computational challenge of social learning.</a></div>
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|
||
<div class="nl"><a target="_blank" href="/pubmed/30078747">Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kahles A,
|
||
Lehmann KV,
|
||
Toussaint NC,
|
||
Hüser M,
|
||
Stark SG,
|
||
Sachsenberg T,
|
||
Stegle O,
|
||
Kohlbacher O,
|
||
Sander C;
|
||
Cancer Genome Atlas Research Network,
|
||
Rätsch G</span><br />
|
||
<span class="medgenPMjournal">Cancer Cell</span>
|
||
2018 Aug 13;34(2):211-224.e6.
|
||
Epub 2018 Aug 2
|
||
doi: 10.1016/j.ccell.2018.07.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30078747" target="_blank">30078747</a><a href="/pmc/articles/PMC9844097" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23652670">Carney complex.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Espiard S,
|
||
Bertherat J</span><br />
|
||
<span class="medgenPMjournal">Front Horm Res</span>
|
||
2013;41:50-62.
|
||
Epub 2013 Mar 19
|
||
doi: 10.1159/000345669.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23652670" target="_blank">23652670</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Carney%20complex%20type%202%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (197)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/36213268">Association between subclinical hyperthyroidism and a PRKAR1A gene variant in Carney complex patients: A case report and systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang H,
|
||
Mao M,
|
||
Liu D,
|
||
Duan L</span><br />
|
||
<span class="medgenPMjournal">Front Endocrinol (Lausanne)</span>
|
||
2022;13:951133.
|
||
Epub 2022 Sep 23
|
||
doi: 10.3389/fendo.2022.951133.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36213268" target="_blank">36213268</a><a href="/pmc/articles/PMC9538310" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34461119">Conjunctival myxoma: A systematic review of a rare tumor.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alvarado-Villacorta R,
|
||
Torres Zavala NM,
|
||
Marroquín Loayza L,
|
||
Rodríguez-Reyes AA</span><br />
|
||
<span class="medgenPMjournal">Surv Ophthalmol</span>
|
||
2022 May-Jun;67(3):729-740.
|
||
Epub 2021 Aug 27
|
||
doi: 10.1016/j.survophthal.2021.08.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34461119" target="_blank">34461119</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34196157">L3 rootlet recurrent melanocytic schwannoma - case report and literature review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Georgiev GK,
|
||
Todorov IV,
|
||
Shamov TP,
|
||
Krushovenski IV,
|
||
Fakirova AD,
|
||
Ilcheva BN,
|
||
Georgiev IT,
|
||
Georgiev ND,
|
||
Prandjev VS,
|
||
Eftimov TN</span><br />
|
||
<span class="medgenPMjournal">Folia Med (Plovdiv)</span>
|
||
2021 Jun 30;63(3):448-456.
|
||
doi: 10.3897/folmed.63.e55295.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34196157" target="_blank">34196157</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28671890">Management of Infected Mesh After Abdominal Hernia Repair: Systematic Review and Single-Institution Experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shubinets V,
|
||
Carney MJ,
|
||
Colen DL,
|
||
Mirzabeigi MN,
|
||
Weissler JM,
|
||
Lanni MA,
|
||
Braslow BM,
|
||
Fischer JP,
|
||
Kovach SJ</span><br />
|
||
<span class="medgenPMjournal">Ann Plast Surg</span>
|
||
2018 Feb;80(2):145-153.
|
||
doi: 10.1097/SAP.0000000000001189.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28671890" target="_blank">28671890</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25639313">Cushing's disease: current medical therapies and molecular insights guiding future therapies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lau D,
|
||
Rutledge C,
|
||
Aghi MK</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Focus</span>
|
||
2015 Feb;38(2):E11.
|
||
doi: 10.3171/2014.10.FOCUS14700.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25639313" target="_blank">25639313</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Carney%20complex%20type%202%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (9)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
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<div class="portlet mgSection" id="ID_113">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul id="my-toc"></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/search?index=entry&start=1&limit=10&sort=score%20desc&field=number&search=605244" target="_blank">OMIM</a></li><li><a href="https://clinicaltrials.gov/search?cond=Carney%20complex%20type%202" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
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</div>
|
||
|
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<div class="portlet mgSection" id="ID_121">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(carney%20complex%20type%202)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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|
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<div class="portlet mgSection" id="ID_115">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Molecular_resources">Molecular resources</h1><a sid="115" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="https://catalog.coriell.org/Search?q=605244" target="_blank">Coriell Institute for Medical Research</a></li></ul></div>
|
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</div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Consumer_resources">Consumer resources</h1><a sid="116" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Carney%20complex%20type%202" target="_blank">MedlinePlus</a></li><li><a href="https://medlineplus.gov/genetics/condition/carney-complex" target="_blank">MedlinePlusGenetics (GHR)</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/15377/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
|
||
</div>
|
||
</div>
|
||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
|
||
<div class="portlet_title">
|
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<h3>Reviews</h3>
|
||
</div>
|
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="Reviews" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter"></a>
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<div class="portlet_content">
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<ul>
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||
<li>
|
||
<a href="/pubmed/20301463" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=3" target="_blank"><span class="gene_reviews">GeneReviews</span></a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed/clinical?term=Carney%20complex%20type%202" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=3" target="_blank">PubMed Clinical Queries</a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed?term=Carney%20complex%20type%202%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=3&linkpostotal=3" target="_blank">Reviews in PubMed</a>
|
||
</li>
|
||
</ul>
|
||
</div>
|
||
</div>
|
||
|
||
<!-- MedGen supplemental column ends here -->
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||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
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<div class="portlet_title">
|
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<h3>Related information</h3>
|
||
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||
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<div class="portlet_content DiscoveryDbLinks">
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<ul>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/mesh?LinkName=medgen_mesh&from_uid=340253" ref="log$=recordlinks">MeSH</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related Medical Subject Headings</div>
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||
</li>
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<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/books?LinkName=medgen_books&from_uid=340253" ref="log$=recordlinks">NCBI Bookshelf</a>
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<div class="brieflinkpop offscreen_noflow">Related information in NCBI Bookshelf</div>
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||
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|
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<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/omim?LinkName=medgen_omim&from_uid=340253" ref="log$=recordlinks">OMIM</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related records in OMIM</div>
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||
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=340253" ref="log$=recordlinks">PMC Articles</a>
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<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=340253" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_bookshelf_cited&from_uid=340253" ref="log$=recordlinks">PubMed (Bookshelf cited)</a>
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<div class="brieflinkpop offscreen_noflow">Links to PubMed based on citations in GeneReviews and Medical Genetics Summaries</div>
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</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_genereviews&from_uid=340253" ref="log$=recordlinks">PubMed (GeneReviews)</a>
|
||
<div class="brieflinkpop offscreen_noflow">GeneReviews in PubMed</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_omim&from_uid=340253" ref="log$=recordlinks">PubMed (OMIM)</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
|
||
</li>
|
||
</ul>
|
||
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|
||
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|
||
|
||
|
||
<div class="portlet">
|
||
<div class="portlet_head">
|
||
<div class="portlet_title">
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<h3>Recent activity</h3>
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<div id="HTDisplay" class="">
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" cmd="ClearHT" href="?cmd=ClearHT&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory">
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||
Clear
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" class="HTOn" cmd="HTOff" href="?cmd=HTOff&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle">
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Turn Off
|
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|
||
<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" sid="2" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" class="HTOff" cmd="HTOn" href="?cmd=HTOn&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle">
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Turn On
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|
||
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|
||
<ul id="activity">
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d35bbb67c23b31e0131936">Carney complex type 2</a>
|
||
<div class="ralinkpop offscreen_noflow">Carney complex type 2<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary">MedGen</div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d35bb767c23b31e012fd7d">Carney complex, type 1</a>
|
||
<div class="ralinkpop offscreen_noflow">Carney complex, type 1<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary">MedGen</div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d35ba167c23b31e012ac7a">Carney Complex - GeneReviews®</a>
|
||
<div class="ralinkpop offscreen_noflow">Carney Complex - GeneReviews®<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary"></div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d35ba084f3725e5998722f">Table B. [OMIM Entries for Carney Complex (View All in OMIM)]. - GeneReviews®</a>
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<div class="ralinkpop offscreen_noflow">RecName: Full=cAMP-dependent protein kinase type I-alpha regulatory subunit; AltName: Full=Tissue-specific extinguisher 1; Short=TSE1<div class="brieflinkpopdesc">gi|125193|sp|P10644.1|KAP0_HUMAN</div></div>
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