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<meta name="keywords" content="C1857779, cep290, cep290 senior-loken syndrome, disease or syndrome, senior-loken syndrome 6, senior-loken syndrome caused by mutation in cep290, senior-loken syndrome type 6, slsn6, 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="Senior-Loken syndrome-6 (SLSN6) is an autosomal recessive disorder characterized by the association of nephronophthisis resulting in end-stage renal disease in the second decade of life with retinal degeneration (Sayer et al., 2006).&#13; For a phenotypic description and a discussion of genetic heterogeneity of Senior-Loken syndrome, see 266900." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Senior-Loken syndrome 6 (Concept Id: C1857779)
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<!--
UID=387907
ConceptID=C1857779
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Senior-Loken syndrome 6<span class="h1sub">(SLSN6)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>387907</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)&#10;Click for more information."><span class="highlight" style="background-color:">C1857779</span></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>SLSN6</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Gene (location):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
Gene(s) directly associated with<br />
this condition or phenotype.</div></td>
<td><a target="_blank" title="CEP290 - ID: 80184 - NCBI Gene" href="/gene/80184" class="medgenPMinfo">CEP290</a> (12q21.32)</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
<td><a href="https://monarchinitiative.org/disease/MONDO:0012433" target="_blank">MONDO:0012433</a></td></tr>
<tr><td>OMIM<span class="superscript">®</span>:</td>
<td><a href="https://omim.org/entry/610189" target="_blank">610189</a></td></tr>
</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>
<div class="portlet mgSection" id="ID_100">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">Senior-Loken syndrome-6 (SLSN6) is an autosomal recessive disorder characterized by the association of nephronophthisis resulting in end-stage renal disease in the second decade of life with retinal degeneration (Sayer et al., 2006).&#13; For a phenotypic description and a discussion of genetic heterogeneity of Senior-Loken syndrome, see 266900. [from <a title="Online Mendelian Inheritance in Man" href="http://www.omim.org" class="defSource" target="_blank">OMIM</a>]</div>
</div>
<div class="portlet mgSection" id="ID_117">
<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>
<div class="portlet_content ln"><div class="mgSection"><strong>From MedlinePlus Genetics</strong><br />Nephronophthisis causes fluid-filled cysts to develop in the kidneys beginning in childhood. These cysts impair kidney function, initially causing increased urine production (polyuria), excessive thirst (polydipsia), general weakness, and extreme tiredness (fatigue). Nephronophthisis leads to end-stage renal disease (ESRD) later in childhood or in adolescence. ESRD is a life-threatening failure of kidney function that occurs when the kidneys are no longer able to filter fluids and waste products from the body effectively.<br /><br />Leber congenital amaurosis primarily affects the retina, which is the specialized tissue at the back of the eye that detects light and color. This condition causes vision problems, including an increased sensitivity to light (photophobia), involuntary movements of the eyes (nystagmus), and extreme farsightedness (hyperopia). Some people with Senior-Løken syndrome develop the signs of Leber congenital amaurosis within the first few years of life, while others do not develop vision problems until later in childhood.<br /><br />Senior-Løken syndrome is a rare disorder characterized by the combination of two specific features: a kidney condition called nephronophthisis and an eye condition known as Leber congenital amaurosis.  <a target="_blank" href="https://medlineplus.gov/genetics/condition/senior-loken-syndrome">https://medlineplus.gov/genetics/condition/senior-loken-syndrome</a></div></div>
</div>
<div class="portlet mgSection" id="ID_102">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
<div class="divPopper rprt" id="clin_384526"><div><strong>Stage 5 chronic kidney disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>384526</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)&#10;Click for more information.">C2316810</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">A degree of kidney failure severe enough to require dialysis or kidney transplantation for survival characterized by a severe reduction in glomerular filtration rate (less than 15 ml/min/1.73 m2) and other manifestations including increased serum creatinine.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/384526">Feature record</a> | <a href="/medgen?term=%22Stage%205%20chronic%20kidney%20disease%22%5BClinical%20Features%5D%20OR%20384526%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_340931"><div><strong>Aplasia/Hypoplasia of the cerebellar vermis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>340931</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)&#10;Click for more information.">C1855676</a></dd><dt><span class="dotprefix"></span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
<div class="spaceAbove">Absence or underdevelopment of the vermis of cerebellum.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/340931">Feature record</a> | <a href="/medgen?term=%22Aplasia%2FHypoplasia%20of%20the%20cerebellar%20vermis%22%5BClinical%20Features%5D%20OR%20340931%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_65889"><div><strong>Reduced visual acuity</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>65889</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)&#10;Click for more information.">C0234632</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">Diminished clarity of vision.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/65889">Feature record</a> | <a href="/medgen?term=%22Reduced%20visual%20acuity%22%5BClinical%20Features%5D%20OR%2065889%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_777085"><div><strong>Visual impairment</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>777085</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)&#10;Click for more information.">C3665347</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">Visual impairment (or vision impairment) is vision loss (of a person) to such a degree as to qualify as an additional support need through a significant limitation of visual capability resulting from either disease, trauma, or congenital or degenerative conditions that cannot be corrected by conventional means, such as refractive correction, medication, or surgery.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/777085">Feature record</a> | <a href="/medgen?term=%22Visual%20impairment%22%5BClinical%20Features%5D%20OR%20777085%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_1632921"><div><strong>Rod-cone dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1632921</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)&#10;Click for more information.">C4551714</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">An inherited retinal disease subtype in which the rod photoreceptors appear to be more severely affected than the cone photoreceptors. Typical presentation is with nyctalopia (due to rod dysfunction) followed by loss of mid-peripheral field of vision, which gradually extends and leaves many patients with a small central island of vision due to the preservation of macular cones.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1632921">Feature record</a> | <a href="/medgen?term=%22Rod-cone%20dystrophy%22%5BClinical%20Features%5D%20OR%201632921%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(&quot;.TreeLite&quot;,&quot;#ID_102&quot;).TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(&quot;.TreeLite&quot;,&quot;#ID_102&quot;).TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of the eye</span><ul><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_65889" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Reduced visual acuity</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_1632921" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Rod-cone dystrophy</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_777085" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Visual impairment</a></span></li></ul></li><li><span class="TLline">Abnormality of the genitourinary system</span><ul><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_384526" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Stage 5 chronic kidney disease</a></span></li></ul></li><li><span class="TLline">Abnormality of the nervous system</span><ul><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_340931" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Aplasia/Hypoplasia of the cerebellar vermis</a></span></li></ul></li></ul></div></div>
</div>
<div class="portlet mgSection" id="ID_118">
<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=C0403553[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=96045">C</a></span><span class="chiclet Rcolor round" title="Research test"><a target="_blank" href="/gtr/tests/?term=C0403553[DISCUI]&amp;test_type=Research&amp;redirect=true" ref="ncbi_uid=96045">R</a></span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=96045" target="_blank" href="/omim/266900">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=96045" ref="ncbi_uid=96045">V</a></span></span><span class="TLline"><a href="/medgen/96045" ref="tree=GTR&amp;ncbi_uid=96045&amp;link_uid=96045" title="View MedGen record for 'Renal dysplasia and retinal aplasia'">Renal dysplasia and retinal aplasia</a></span><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C4551559[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=1639722">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=1639722" target="_blank" href="/omim/266900">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=1639722" ref="ncbi_uid=1639722">V</a></span></span><span class="TLline"><a href="/medgen/1639722" ref="tree=GTR&amp;ncbi_uid=1639722&amp;link_uid=1639722" title="View MedGen record for 'Senior-Loken syndrome 1'">Senior-Loken syndrome 1</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1846980[DISCUI]&amp;test_type=Clinical&amp;redirect=true" ref="ncbi_uid=335569">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=335569" target="_blank" href="/omim/606995">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=335569" ref="ncbi_uid=335569">V</a></span></span><span class="TLline"><a href="/medgen/335569" ref="tree=GTR&amp;ncbi_uid=335569&amp;link_uid=335569" title="View MedGen record for 'Senior-loken syndrome 3'">Senior-loken syndrome 3</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1846979[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=337697">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=337697" target="_blank" href="/omim/606996">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=337697" ref="ncbi_uid=337697">V</a></span></span><span class="TLline"><a href="/medgen/337697" ref="tree=GTR&amp;ncbi_uid=337697&amp;link_uid=337697" title="View MedGen record for 'Senior-Loken syndrome 4'">Senior-Loken syndrome 4</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1836517[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=332226">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=332226" target="_blank" href="/omim/609237">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=332226" ref="ncbi_uid=332226">V</a></span></span><span class="TLline"><a href="/medgen/332226" ref="tree=GTR&amp;ncbi_uid=332226&amp;link_uid=332226" title="View MedGen record for 'Senior-Loken syndrome 5'">Senior-Loken syndrome 5</a></span></li><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1857779[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=387907">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=387907" target="_blank" href="/omim/610142">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=387907" ref="ncbi_uid=387907">V</a></span></span><span class="TLline">Senior-Loken syndrome 6</span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C3150877[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=462227">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=462227" target="_blank" href="/omim/613524">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=462227" ref="ncbi_uid=462227">V</a></span></span><span class="TLline"><a href="/medgen/462227" ref="tree=GTR&amp;ncbi_uid=462227&amp;link_uid=462227" title="View MedGen record for 'Senior-Loken syndrome 7'">Senior-Loken syndrome 7</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C4225376[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=905171">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=905171" target="_blank" href="/omim/608151">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=905171" ref="ncbi_uid=905171">V</a></span></span><span class="TLline"><a href="/medgen/905171" ref="tree=GTR&amp;ncbi_uid=905171&amp;link_uid=905171" title="View MedGen record for 'Senior-Loken syndrome 8'">Senior-Loken syndrome 8</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C4225263[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=899086">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=899086" target="_blank" href="/omim/607380">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=899086" ref="ncbi_uid=899086">V</a></span></span><span class="TLline"><a href="/medgen/899086" ref="tree=GTR&amp;ncbi_uid=899086&amp;link_uid=899086" title="View MedGen record for 'Senior-Loken syndrome 9'">Senior-Loken syndrome 9</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/1842297" ref="tree=MeSH" title="MedGen record for Familial cystic renal disease">Familial cystic renal disease</a></span><ul><li><span class="TLline"><a href="/medgen/96045" ref="tree=MeSH" title="MedGen record for Renal dysplasia and retinal aplasia">Renal dysplasia and retinal aplasia</a></span><ul><li><span class="matched_ds">Senior-Loken syndrome 6</span></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/20683928">Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Coppieters F,
Casteels I,
Meire F,
De Jaegere S,
Hooghe S,
van Regemorter N,
Van Esch H,
Matuleviciene A,
Nunes L,
Meersschaut V,
Walraedt S,
Standaert L,
Coucke P,
Hoeben H,
Kroes HY,
Vande Walle J,
de Ravel T,
Leroy BP,
De Baere E</span><br />
<span class="medgenPMjournal">Hum Mutat</span>
2010 Oct;31(10):E1709-66.
doi: 10.1002/humu.21336.
<span class="bold">PMID: </span><a href="/pubmed/20683928" target="_blank">20683928</a><a href="/pmc/articles/PMC3048164" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(senior-loken%20syndrome%206)%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 (1)</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/36990420">Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
Li S,
Jiang Y,
Wang Y,
Ouyang J,
Yi Z,
Sun W,
Jia X,
Xiao X,
Wang P,
Zhang Q</span><br />
<span class="medgenPMjournal">Am J Ophthalmol</span>
2023 Aug;252:188-204.
Epub 2023 Mar 27
doi: 10.1016/j.ajo.2023.03.025.
<span class="bold">PMID: </span><a href="/pubmed/36990420" target="_blank">36990420</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33512896">SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yahalom C,
Volovelsky O,
Macarov M,
Altalbishi A,
Alsweiti Y,
Schneider N,
Hanany M,
Khan MI,
Cremers FPM,
Anteby I,
Banin E,
Sharon D,
Khateb S</span><br />
<span class="medgenPMjournal">Retina</span>
2021 Oct 1;41(10):2179-2187.
doi: 10.1097/IAE.0000000000003138.
<span class="bold">PMID: </span><a href="/pubmed/33512896" target="_blank">33512896</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32165824">Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Surl D,
Shin S,
Lee ST,
Choi JR,
Lee J,
Byeon SH,
Han SH,
Lim HT,
Han J</span><br />
<span class="medgenPMjournal">Mol Vis</span>
2020;26:26-35.
Epub 2020 Feb 24
<span class="bold">PMID: </span><a href="/pubmed/32165824" target="_blank">32165824</a><a href="/pmc/articles/PMC7043639" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/19508969">Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Otto EA,
Tory K,
Attanasio M,
Zhou W,
Chaki M,
Paruchuri Y,
Wise EL,
Wolf MT,
Utsch B,
Becker C,
Nürnberg G,
Nürnberg P,
Nayir A,
Saunier S,
Antignac C,
Hildebrandt F</span><br />
<span class="medgenPMjournal">J Med Genet</span>
2009 Oct;46(10):663-70.
Epub 2009 Jun 8
doi: 10.1136/jmg.2009.066613.
<span class="bold">PMID: </span><a href="/pubmed/19508969" target="_blank">19508969</a></div>
<div class="nl"><a target="_blank" href="/pubmed/8250041">Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study Group.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hildebrandt F,
Singh-Sawhney I,
Schnieders B,
Centofante L,
Omran H,
Pohlmann A,
Schmaltz C,
Wedekind H,
Schubotz C,
Antignac C</span><br />
<span class="medgenPMjournal">Am J Hum Genet</span>
1993 Dec;53(6):1256-61.
<span class="bold">PMID: </span><a href="/pubmed/8250041" target="_blank">8250041</a><a href="/pmc/articles/PMC1682479" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Senior-Loken%20syndrome%206%22%20AND%20Etiology%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 (5)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/39213781">Spectrum and frequencies of extraocular features reported in CEP290-associated ciliopathy - A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vrabič N,
Fakin A,
Tekavčič Pompe M</span><br />
<span class="medgenPMjournal">J Fr Ophtalmol</span>
2024 Oct;47(8):104232.
Epub 2024 Aug 29
doi: 10.1016/j.jfo.2024.104232.
<span class="bold">PMID: </span><a href="/pubmed/39213781" target="_blank">39213781</a></div>
<div class="nl"><a target="_blank" href="/pubmed/36990420">Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
Li S,
Jiang Y,
Wang Y,
Ouyang J,
Yi Z,
Sun W,
Jia X,
Xiao X,
Wang P,
Zhang Q</span><br />
<span class="medgenPMjournal">Am J Ophthalmol</span>
2023 Aug;252:188-204.
Epub 2023 Mar 27
doi: 10.1016/j.ajo.2023.03.025.
<span class="bold">PMID: </span><a href="/pubmed/36990420" target="_blank">36990420</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33512896">SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yahalom C,
Volovelsky O,
Macarov M,
Altalbishi A,
Alsweiti Y,
Schneider N,
Hanany M,
Khan MI,
Cremers FPM,
Anteby I,
Banin E,
Sharon D,
Khateb S</span><br />
<span class="medgenPMjournal">Retina</span>
2021 Oct 1;41(10):2179-2187.
doi: 10.1097/IAE.0000000000003138.
<span class="bold">PMID: </span><a href="/pubmed/33512896" target="_blank">33512896</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32165824">Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Surl D,
Shin S,
Lee ST,
Choi JR,
Lee J,
Byeon SH,
Han SH,
Lim HT,
Han J</span><br />
<span class="medgenPMjournal">Mol Vis</span>
2020;26:26-35.
Epub 2020 Feb 24
<span class="bold">PMID: </span><a href="/pubmed/32165824" target="_blank">32165824</a><a href="/pmc/articles/PMC7043639" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/1840995">Leber's congenital amaurosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">De Laey JJ</span><br />
<span class="medgenPMjournal">Bull Soc Belge Ophtalmol</span>
1991;241:41-50.
<span class="bold">PMID: </span><a href="/pubmed/1840995" target="_blank">1840995</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Senior-Loken%20syndrome%206%22%20AND%20Diagnosis%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 (11)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/32279418">Threatening drug-drug interaction in a kidney transplant patient with coronavirus disease 2019 (COVID-19).</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bartiromo M,
Borchi B,
Botta A,
Bagalà A,
Lugli G,
Tilli M,
Cavallo A,
Xhaferi B,
Cutruzzulà R,
Vaglio A,
Bresci S,
Larti A,
Bartoloni A,
Cirami C</span><br />
<span class="medgenPMjournal">Transpl Infect Dis</span>
2020 Aug;22(4):e13286.
Epub 2020 Jul 14
doi: 10.1111/tid.13286.
<span class="bold">PMID: </span><a href="/pubmed/32279418" target="_blank">32279418</a><a href="/pmc/articles/PMC7262190" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Senior-Loken%20syndrome%206%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 (1)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/39806488">Unraveling the genetic spectrum of inherited deaf-blindness in Portugal.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Machado T,
Cortinhal T,
Carvalho AL,
Teixeira-Marques F,
Silva R,
Murta J,
Marques JP</span><br />
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
2025 Jan 14;20(1):22.
doi: 10.1186/s13023-025-03542-5.
<span class="bold">PMID: </span><a href="/pubmed/39806488" target="_blank">39806488</a><a href="/pmc/articles/PMC11730510" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/39213781">Spectrum and frequencies of extraocular features reported in CEP290-associated ciliopathy - A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vrabič N,
Fakin A,
Tekavčič Pompe M</span><br />
<span class="medgenPMjournal">J Fr Ophtalmol</span>
2024 Oct;47(8):104232.
Epub 2024 Aug 29
doi: 10.1016/j.jfo.2024.104232.
<span class="bold">PMID: </span><a href="/pubmed/39213781" target="_blank">39213781</a></div>
<div class="nl"><a target="_blank" href="/pubmed/24674142">Clinical features and mutation of NPHP5 in two Chinese siblings with Senior-Løken syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tong H,
Yue Z,
Sun L,
Chen H,
Wang W,
Wang H</span><br />
<span class="medgenPMjournal">Nephrology (Carlton)</span>
2013 Dec;18(12):838-42.
doi: 10.1111/nep.12156.
<span class="bold">PMID: </span><a href="/pubmed/24674142" target="_blank">24674142</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Senior-Loken%20syndrome%206%22%20AND%20Prognosis%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 (3)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/39213781">Spectrum and frequencies of extraocular features reported in CEP290-associated ciliopathy - A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vrabič N,
Fakin A,
Tekavčič Pompe M</span><br />
<span class="medgenPMjournal">J Fr Ophtalmol</span>
2024 Oct;47(8):104232.
Epub 2024 Aug 29
doi: 10.1016/j.jfo.2024.104232.
<span class="bold">PMID: </span><a href="/pubmed/39213781" target="_blank">39213781</a></div>
<div class="nl"><a target="_blank" href="/pubmed/36990420">Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
Li S,
Jiang Y,
Wang Y,
Ouyang J,
Yi Z,
Sun W,
Jia X,
Xiao X,
Wang P,
Zhang Q</span><br />
<span class="medgenPMjournal">Am J Ophthalmol</span>
2023 Aug;252:188-204.
Epub 2023 Mar 27
doi: 10.1016/j.ajo.2023.03.025.
<span class="bold">PMID: </span><a href="/pubmed/36990420" target="_blank">36990420</a></div>
<div class="nl"><a target="_blank" href="/pubmed/24674142">Clinical features and mutation of NPHP5 in two Chinese siblings with Senior-Løken syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tong H,
Yue Z,
Sun L,
Chen H,
Wang W,
Wang H</span><br />
<span class="medgenPMjournal">Nephrology (Carlton)</span>
2013 Dec;18(12):838-42.
doi: 10.1111/nep.12156.
<span class="bold">PMID: </span><a href="/pubmed/24674142" target="_blank">24674142</a></div>
<div class="nl"><a target="_blank" href="/pubmed/19508969">Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Otto EA,
Tory K,
Attanasio M,
Zhou W,
Chaki M,
Paruchuri Y,
Wise EL,
Wolf MT,
Utsch B,
Becker C,
Nürnberg G,
Nürnberg P,
Nayir A,
Saunier S,
Antignac C,
Hildebrandt F</span><br />
<span class="medgenPMjournal">J Med Genet</span>
2009 Oct;46(10):663-70.
Epub 2009 Jun 8
doi: 10.1136/jmg.2009.066613.
<span class="bold">PMID: </span><a href="/pubmed/19508969" target="_blank">19508969</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18607645">Nephronophthisis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Salomon R,
Saunier S,
Niaudet P</span><br />
<span class="medgenPMjournal">Pediatr Nephrol</span>
2009 Dec;24(12):2333-44.
Epub 2008 Jul 8
doi: 10.1007/s00467-008-0840-z.
<span class="bold">PMID: </span><a href="/pubmed/18607645" target="_blank">18607645</a><a href="/pmc/articles/PMC2770134" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Senior-Loken%20syndrome%206%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 (8)</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/39213781">Spectrum and frequencies of extraocular features reported in CEP290-associated ciliopathy - A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vrabič N,
Fakin A,
Tekavčič Pompe M</span><br />
<span class="medgenPMjournal">J Fr Ophtalmol</span>
2024 Oct;47(8):104232.
Epub 2024 Aug 29
doi: 10.1016/j.jfo.2024.104232.
<span class="bold">PMID: </span><a href="/pubmed/39213781" target="_blank">39213781</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Senior-Loken%20syndrome%206%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 (1)</a></div></div>
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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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>
<div class="portlet_content ln"><ul id="my-toc"></ul></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C1857779%5bDISCUI%5d&amp;filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (64)</a></li>
<li><a href="/gtr/tests?term=C1857779%5bDISCUI%5d&amp;filter=method%3A2%5F9" target="_blank">Sequence analysis of select exons (1)</a></li>
<li><a href="/gtr/tests?term=C1857779%5bDISCUI%5d&amp;filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (70)</a></li>
<li><a href="/gtr/tests?term=C1857779%5bDISCUI%5d&amp;filter=method%3A2%5F19" target="_blank">Targeted variant analysis (12)</a></li>
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C1857779%5bDISCUI%5d" target="_blank">See all (84)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/search?index=entry&amp;start=1&amp;limit=10&amp;sort=score%20desc&amp;field=number&amp;search=610189" target="_blank">OMIM</a></li><li><a href="https://clinicaltrials.gov/search?cond=Senior-Loken%20syndrome%206" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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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>
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(senior-loken%20syndrome%206)%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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<div class="portlet_content ln"><ul><li><a href="http://www.omim.org/search?index=entry&amp;start=1&amp;limit=10&amp;sort=score%20desc&amp;field=number&amp;search=610142" target="_blank">OMIM</a></li><li><a href="/clinvar/?term=80184[geneid]" target="_blank">View CEP290 variations in ClinVar</a></li><li><a href="/nuccore/197313679" target="_blank">RefSeqGene</a></li><li><a href="https://catalog.coriell.org/Search?q=610189" target="_blank">Coriell Institute for Medical Research</a></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://www.malacards.org/card/senior_loken_syndrome_6" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&amp;query=Senior-Loken%20syndrome%206" target="_blank">MedlinePlus</a></li><li><a href="https://medlineplus.gov/genetics/condition/senior-loken-syndrome" target="_blank">MedlinePlusGenetics (GHR)</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/15476/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
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