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<!--
|
||
UID=8649
|
||
ConceptID=C0014394
|
||
-->
|
||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Enuresis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>8649</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.">C0014394</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>enuresis</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0000805">HP:0000805</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
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<td><a href="https://monarchinitiative.org/disease/MONDO:0024290" target="_blank">MONDO:0024290</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_100">
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<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">Lack of the ability to control the urinary bladder leading to involuntary urination at an age where control of the bladder should already be possible. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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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>
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<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="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0014394[DISCUI]&test_type=Clinical&redirect=true" ref="ncbi_uid=8649">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=8649" ref="ncbi_uid=8649">V</a></span></span><span class="TLline">Enuresis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868417" ref="tree=MeSH" title="MedGen record for Abnormal nervous system physiology">Abnormal nervous system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/868938" ref="tree=MeSH" title="MedGen record for Abnormality of mental function">Abnormality of mental function</a></span><ul><li><span class="TLline"><a href="/medgen/14048" ref="tree=MeSH" title="MedGen record for Atypical behavior">Atypical behavior</a></span><ul><li><span class="matched_ds">Enuresis</span><ul><li><span class="TLline"><a href="/medgen/78718" ref="tree=MeSH" title="MedGen record for Daytime enuresis">Daytime enuresis</a></span></li><li><span class="TLline"><a href="/medgen/869320" ref="tree=MeSH" title="MedGen record for Enuresis diurna">Enuresis diurna</a></span></li><li><span class="TLline"><a href="/medgen/124355" ref="tree=MeSH" title="MedGen record for Nocturnal enuresis">Nocturnal enuresis</a></span></li><li><span class="TLline"><a href="/medgen/4802" ref="tree=MeSH" title="MedGen record for Nonorganic Enuresis">Nonorganic Enuresis</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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||
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||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_59799"><div><strong>Williams syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>59799</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.">C0175702</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Williams syndrome (WS) is characterized by developmental delay, intellectual disability (usually mild), a specific cognitive profile, unique personality characteristics, cardiovascular disease (supravalvar aortic stenosis, peripheral pulmonary stenosis, hypertension), connective tissue abnormalities, growth deficiency, endocrine abnormalities (early puberty, hypercalcemia, hypercalciuria, hypothyroidism), and distinctive facies. Hypotonia and hyperextensible joints can result in delayed attainment of motor milestones. Feeding difficulties often lead to poor weight gain in infancy.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/59799">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75681"><div><strong>Familial hypokalemia-hypomagnesemia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75681</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.">C0268450</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Gitelman syndrome (GTLMNS) is an autosomal recessive renal tubular salt-wasting disorder characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. It is the most common renal tubular disorder among Caucasians (prevalence of 1 in 40,000). Most patients have onset of symptoms as adults, but some present in childhood. Clinical features include transient periods of muscle weakness and tetany, abdominal pains, and chondrocalcinosis (summary by Glaudemans et al., 2012). Gitelman syndrome is sometimes referred to as a mild variant of classic Bartter syndrome (607364). For a discussion of genetic heterogeneity of Bartter syndrome, see 607364.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75681">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_98015"><div><strong>Ochoa syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>98015</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.">C0403555</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Urofacial syndrome (UFS; also known as Ochoa syndrome) is characterized by prenatal or childhood onset of urinary bladder voiding dysfunction, abnormal facial movement with expression (resulting from abnormal co-contraction of the corners of the mouth and eyes), and often bowel dysfunction (constipation and/or encopresis). Bladder voiding dysfunction can present before birth as megacystis. In infancy and later childhood, UFS can present with a poor urinary stream and dribbling incontinence; incomplete bladder emptying can lead to urinary infection with progressive kidney failure. Investigations after birth can show abnormal bladder contractility and vesicoureteral reflux of urine into the ureter and renal pelvis. Nocturnal lagophthalmos (incomplete closing of the eyes during sleep) has also been documented.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/98015">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_335569"><div><strong>Senior-loken syndrome 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>335569</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.">C1846980</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">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.\n\nSenior-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.\n\nLeber 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.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/335569">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_346809"><div><strong>Nephronophthisis 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>346809</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.">C1858392</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Nephronophthisis can occur as part of separate syndromes that affect other areas of the body; these are often referred to as nephronophthisis-associated ciliopathies. For example, Senior-Løken syndrome is characterized by the combination of nephronophthisis and a breakdown of the light-sensitive tissue at the back of the eye (retinal degeneration); Joubert syndrome affects many parts of the body, causing neurological problems and other features, which can include nephronophthisis.\n\nAbout 85 percent of all cases of nephronophthisis are isolated, which means they occur without other signs and symptoms. Some people with nephronophthisis have additional features, which can include liver fibrosis, heart abnormalities, or mirror image reversal of the position of one or more organs inside the body (situs inversus).\n\nNephronophthisis eventually leads to end-stage renal disease (ESRD), 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. Nephronophthisis can be classified by the approximate age at which ESRD begins: around age 1 (infantile), around age 13 (juvenile), and around age 19 (adolescent).\n\nNephronophthisis is a disorder that affects the kidneys. It is characterized by inflammation and scarring (fibrosis) that impairs kidney function. These abnormalities lead to increased urine production (polyuria), excessive thirst (polydipsia), general weakness, and extreme tiredness (fatigue). In addition, affected individuals develop fluid-filled cysts in the kidneys, usually in an area known as the corticomedullary region. Another feature of nephronophthisis is a shortage of red blood cells, a condition known as anemia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/346809">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_350085"><div><strong>Spinocerebellar ataxia type 29</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>350085</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.">C1861732</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spinocerebellar ataxia-29 (SCA29) is an autosomal dominant neurologic disorder characterized by onset in infancy of delayed motor development and mild cognitive delay. Affected individuals develop a very slowly progressive or nonprogressive gait and limb ataxia associated with cerebellar atrophy on brain imaging. Additional variable features include nystagmus, dysarthria, and tremor (summary by Huang et al., 2012). For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/350085">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_411243"><div><strong>EAST syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>411243</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.">C2748572</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Syndrome with characteristics of seizures, sensorineural deafness, ataxia, intellectual deficit, and electrolyte imbalance. It has been described in five patients from four families. The disease is caused by homozygous or compound heterozygous mutations in the KCNJ10 gene, encoding a potassium channel expressed in the brain, spinal cord, inner ear and kidneys. Transmission is autosomal recessive.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/411243">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_419162"><div><strong>Amelogenesis imperfecta type 1G</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>419162</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.">C2931783</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Amelogenesis imperfecta and gingival fibromatosis syndrome is an autosomal recessive condition characterized by mild gingival fibromatosis and dental anomalies, including hypoplastic amelogenesis imperfecta, intrapulpal calcifications, delay of tooth eruption, hypodontia/oligodontia, pericoronal radiolucencies, and unerupted teeth (Martelli-Junior et al., 2008).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/419162">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_477074"><div><strong>Intellectual disability, X-linked 90</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>477074</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.">C3275443</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the DLG3 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/477074">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_767434"><div><strong>Urofacial syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>767434</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.">C3554520</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Urofacial syndrome (UFS; also known as Ochoa syndrome) is characterized by prenatal or childhood onset of urinary bladder voiding dysfunction, abnormal facial movement with expression (resulting from abnormal co-contraction of the corners of the mouth and eyes), and often bowel dysfunction (constipation and/or encopresis). Bladder voiding dysfunction can present before birth as megacystis. In infancy and later childhood, UFS can present with a poor urinary stream and dribbling incontinence; incomplete bladder emptying can lead to urinary infection with progressive kidney failure. Investigations after birth can show abnormal bladder contractility and vesicoureteral reflux of urine into the ureter and renal pelvis. Nocturnal lagophthalmos (incomplete closing of the eyes during sleep) has also been documented.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/767434">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_862201"><div><strong>Intellectual disability-severe speech delay-mild dysmorphism syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>862201</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.">C4013764</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">FOXP1 syndrome is characterized by delays in early motor and language milestones, mild-to-severe intellectual deficits, speech and language impairment in all individuals regardless of level of cognitive abilities, and behavior abnormalities (including autism spectrum disorder or autistic features, attention-deficit/hyperactivity disorder, anxiety, repetitive behaviors, sleep disturbances, and sensory symptoms). Other common findings are oromotor dysfunction (contributing to speech and feeding difficulties), refractive errors, strabismus, cardiac abnormalities, renal abnormalities, cryptorchidism, hypertonia, hearing loss, and epilepsy. To date, more than 200 individuals have been identified with FOXP1 syndrome.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/862201">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_864147"><div><strong>Tenorio syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>864147</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.">C4015710</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Tenorio syndrome (TNORS) is characterized by overgrowth, macrocephaly, and impaired intellectual development. Some patients may have mild hydrocephaly, hypoglycemia, and inflammatory diseases resembling Sjogren syndrome (270150) (summary by Tenorio et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/864147">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1779966"><div><strong>Blepharophimosis-impaired intellectual development syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1779966</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.">C5443984</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Blepharophimosis-impaired intellectual development syndrome (BIS) is a congenital disorder characterized by a distinct facial appearance with blepharophimosis and global development delay. Affected individuals have delayed motor skills, sometimes with inability to walk, and impaired intellectual development with poor or absent speech; some patients show behavioral abnormalities. There are recognizable facial features, including epicanthal folds, sparse eyebrows, broad nasal bridge, short nose with downturned tip, and open mouth with thin upper lip. Other more variable features include distal skeletal anomalies, feeding difficulties with poor growth, respiratory infections, and hypotonia with peripheral spasticity (summary by Cappuccio et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1779966">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794194"><div><strong>Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794194</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.">C5561984</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities (NECRC) is an autosomal dominant disorder characterized by dysmorphic craniofacial features associated with mild developmental delay, mildly impaired intellectual development or learning difficulties, speech delay, and behavioral abnormalities. About half of patients have congenital anomalies of the kidney and urinary tract (CAKUT) and/or congenital cardiac defects, including septal defects (Connaughton et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794194">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1806598"><div><strong>Combined oxidative phosphorylation deficiency 55</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1806598</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.">C5676915</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Combined oxidative phosphorylation deficiency-55 (COXPD55) is characterized by global developmental delay, hypotonia, short stature, and impaired intellectual development with speech disabilities in childhood. Indolent progressive external ophthalmoplegia phenotype has been described in 1 patient (summary by Olahova et al., 2021). For a discussion of genetic heterogeneity of combined oxidative phosphorylation deficiency, see COXPD1 (609060).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1806598">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1840225"><div><strong>Intellectual developmental disorder, X-linked 112</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1840225</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.">C5829589</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">X-linked intellectual disorder-112 (XLID112) is a neurodevelopmental disorder characterized by developmental delay, with speech delay more prominent than motor delay, autism or autism traits, and variable dysmorphic features. Affected females have been reported, which appears to be related to skewed X-inactivation (summary by Hiatt et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1840225">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_419162" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Amelogenesis imperfecta type 1G</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1779966" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Blepharophimosis-impaired intellectual development syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1806598" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Combined oxidative phosphorylation deficiency 55</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_411243" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">EAST syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75681" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial hypokalemia-hypomagnesemia</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (16)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1840225" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder, X-linked 112</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_477074" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, X-linked 90</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_862201" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability-severe speech delay-mild dysmorphism syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_346809" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nephronophthisis 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794194" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_98015" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ochoa syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_335569" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Senior-loken syndrome 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_350085" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 29</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_864147" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Tenorio syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_767434" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Urofacial syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_59799" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Williams syndrome</a></div></span></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/32278657">Management and treatment of nocturnal enuresis-an updated standardization document from the International Children's Continence Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nevéus T,
|
||
Fonseca E,
|
||
Franco I,
|
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Kawauchi A,
|
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Kovacevic L,
|
||
Nieuwhof-Leppink A,
|
||
Raes A,
|
||
Tekgül S,
|
||
Yang SS,
|
||
Rittig S</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Urol</span>
|
||
2020 Feb;16(1):10-19.
|
||
Epub 2020 Jan 30
|
||
doi: 10.1016/j.jpurol.2019.12.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32278657" target="_blank">32278657</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30921525">Clinical Practice Guideline: Tonsillectomy in Children (Update)-Executive Summary.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mitchell RB,
|
||
Archer SM,
|
||
Ishman SL,
|
||
Rosenfeld RM,
|
||
Coles S,
|
||
Finestone SA,
|
||
Friedman NR,
|
||
Giordano T,
|
||
Hildrew DM,
|
||
Kim TW,
|
||
Lloyd RM,
|
||
Parikh SR,
|
||
Shulman ST,
|
||
Walner DL,
|
||
Walsh SA,
|
||
Nnacheta LC</span><br />
|
||
<span class="medgenPMjournal">Otolaryngol Head Neck Surg</span>
|
||
2019 Feb;160(2):187-205.
|
||
doi: 10.1177/0194599818807917.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30921525" target="_blank">30921525</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30798778">Clinical Practice Guideline: Tonsillectomy in Children (Update).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mitchell RB,
|
||
Archer SM,
|
||
Ishman SL,
|
||
Rosenfeld RM,
|
||
Coles S,
|
||
Finestone SA,
|
||
Friedman NR,
|
||
Giordano T,
|
||
Hildrew DM,
|
||
Kim TW,
|
||
Lloyd RM,
|
||
Parikh SR,
|
||
Shulman ST,
|
||
Walner DL,
|
||
Walsh SA,
|
||
Nnacheta LC</span><br />
|
||
<span class="medgenPMjournal">Otolaryngol Head Neck Surg</span>
|
||
2019 Feb;160(1_suppl):S1-S42.
|
||
doi: 10.1177/0194599818801757.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30798778" target="_blank">30798778</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22enuresis%22%5Btiab%3A~0%5D)%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 (497)</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/38368063">Sleep-Related Urologic Dysfunction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Silvestri R</span><br />
|
||
<span class="medgenPMjournal">Sleep Med Clin</span>
|
||
2024 Mar;19(1):169-176.
|
||
Epub 2023 Nov 13
|
||
doi: 10.1016/j.jsmc.2023.10.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38368063" target="_blank">38368063</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35258343">Factors associated with response to simple behavioral intervention in primary enuresis nocturna.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aral A,
|
||
Usta MB,
|
||
Erguner Aral A</span><br />
|
||
<span class="medgenPMjournal">Bull Menninger Clin</span>
|
||
2022 Winter;86(1):67-89.
|
||
doi: 10.1521/bumc.2022.86.1.67.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35258343" target="_blank">35258343</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33012049">Non-dipping phenomenon effects in monosymptomatic nocturnal enuresis treatment?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Çelakıl M</span><br />
|
||
<span class="medgenPMjournal">Pediatr Int</span>
|
||
2021 May;63(5):565-569.
|
||
Epub 2021 Apr 28
|
||
doi: 10.1111/ped.14494.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33012049" target="_blank">33012049</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32278657">Management and treatment of nocturnal enuresis-an updated standardization document from the International Children's Continence Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nevéus T,
|
||
Fonseca E,
|
||
Franco I,
|
||
Kawauchi A,
|
||
Kovacevic L,
|
||
Nieuwhof-Leppink A,
|
||
Raes A,
|
||
Tekgül S,
|
||
Yang SS,
|
||
Rittig S</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Urol</span>
|
||
2020 Feb;16(1):10-19.
|
||
Epub 2020 Jan 30
|
||
doi: 10.1016/j.jpurol.2019.12.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32278657" target="_blank">32278657</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12722850">Nocturnal enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Thiedke CC</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2003 Apr 1;67(7):1499-506.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12722850" target="_blank">12722850</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Enuresis%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 (1787)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39085181">Nocturnal Enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Guzman JA,
|
||
Palmer LS</span><br />
|
||
<span class="medgenPMjournal">Pediatr Rev</span>
|
||
2024 Aug 1;45(8):479-481.
|
||
doi: 10.1542/pir.2023-006166.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39085181" target="_blank">39085181</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31030825">Nocturnal Enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Walker RA</span><br />
|
||
<span class="medgenPMjournal">Prim Care</span>
|
||
2019 Jun;46(2):243-248.
|
||
doi: 10.1016/j.pop.2019.02.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31030825" target="_blank">31030825</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28888814">Primary and Secondary Enuresis: Pathophysiology, Diagnosis, and Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Haid B,
|
||
Tekgül S</span><br />
|
||
<span class="medgenPMjournal">Eur Urol Focus</span>
|
||
2017 Apr;3(2-3):198-206.
|
||
Epub 2017 Sep 6
|
||
doi: 10.1016/j.euf.2017.08.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28888814" target="_blank">28888814</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19411333">Enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Graham KM,
|
||
Levy JB</span><br />
|
||
<span class="medgenPMjournal">Pediatr Rev</span>
|
||
2009 May;30(5):165-72; quiz 173.
|
||
doi: 10.1542/pir.30-5-165.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19411333" target="_blank">19411333</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3309849">Incontinence and enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McLorie GA,
|
||
Husmann DA</span><br />
|
||
<span class="medgenPMjournal">Pediatr Clin North Am</span>
|
||
1987 Oct;34(5):1159-74.
|
||
doi: 10.1016/s0031-3955(16)36324-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3309849" target="_blank">3309849</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Enuresis%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 (1220)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34358324">Once-nightly sodium oxybate (FT218) demonstrated improvement of symptoms in a phase 3 randomized clinical trial in patients with narcolepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kushida CA,
|
||
Shapiro CM,
|
||
Roth T,
|
||
Thorpy MJ,
|
||
Corser BC,
|
||
Ajayi AO,
|
||
Rosenberg R,
|
||
Roy A,
|
||
Seiden D,
|
||
Dubow J,
|
||
Dauvilliers Y</span><br />
|
||
<span class="medgenPMjournal">Sleep</span>
|
||
2022 Jun 13;45(6)
|
||
doi: 10.1093/sleep/zsab200.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34358324" target="_blank">34358324</a><a href="/pmc/articles/PMC9189976" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31395789">Common urological problems in children: primary nocturnal enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chan IHY,
|
||
Wong KKY</span><br />
|
||
<span class="medgenPMjournal">Hong Kong Med J</span>
|
||
2019 Aug;25(4):305-11.
|
||
Epub 2019 Aug 5
|
||
doi: 10.12809/hkmj197916.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31395789" target="_blank">31395789</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27343233">Desmopressin Withdrawal Strategy for Pediatric Enuresis: A Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chua ME,
|
||
Silangcruz JM,
|
||
Chang SJ,
|
||
Williams K,
|
||
Saunders M,
|
||
Lopes RI,
|
||
Farhat WA,
|
||
Yang SS</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
|
||
2016 Jul;138(1)
|
||
Epub 2016 Jun 24
|
||
doi: 10.1542/peds.2016-0495.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27343233" target="_blank">27343233</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22844682">Neuroleptics: bedwetting.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Prescrire Int</span>
|
||
2012 May;21(127):129.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22844682" target="_blank">22844682</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6339023">A guide to the pharmacology of placebos.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gowdey CW</span><br />
|
||
<span class="medgenPMjournal">Can Med Assoc J</span>
|
||
1983 Apr 15;128(8):921-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6339023" target="_blank">6339023</a><a href="/pmc/articles/PMC1875414" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Enuresis%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 (1490)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/22669134">Diaphragmatic breathing exercises and pelvic floor retraining in children with dysfunctional voiding.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zivkovic V,
|
||
Lazovic M,
|
||
Vlajkovic M,
|
||
Slavkovic A,
|
||
Dimitrijevic L,
|
||
Stankovic I,
|
||
Vacic N</span><br />
|
||
<span class="medgenPMjournal">Eur J Phys Rehabil Med</span>
|
||
2012 Sep;48(3):413-21.
|
||
Epub 2012 Jun 5
|
||
<span class="bold">PMID: </span><a href="/pubmed/22669134" target="_blank">22669134</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16719255">Nocturnal enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Makari J,
|
||
Rushton HG</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2006 May 1;73(9):1611-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16719255" target="_blank">16719255</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10914301">Secondary nocturnal enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Robson WL,
|
||
Leung AK</span><br />
|
||
<span class="medgenPMjournal">Clin Pediatr (Phila)</span>
|
||
2000 Jul;39(7):379-85.
|
||
doi: 10.1177/000992280003900701.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10914301" target="_blank">10914301</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4680217">Aversion therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McConaghy N</span><br />
|
||
<span class="medgenPMjournal">Semin Psychiatry</span>
|
||
1972 May;4(2):139-44.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4680217" target="_blank">4680217</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4942939">Hemorrhoidectomy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Parks AG</span><br />
|
||
<span class="medgenPMjournal">Adv Surg</span>
|
||
1971;5:1-50.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4942939" target="_blank">4942939</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Enuresis%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 (736)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35258343">Factors associated with response to simple behavioral intervention in primary enuresis nocturna.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aral A,
|
||
Usta MB,
|
||
Erguner Aral A</span><br />
|
||
<span class="medgenPMjournal">Bull Menninger Clin</span>
|
||
2022 Winter;86(1):67-89.
|
||
doi: 10.1521/bumc.2022.86.1.67.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35258343" target="_blank">35258343</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26555692">Undiagnosed neurological disease as a potential cause of male lower urinary tract symptoms.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wei DY,
|
||
Drake MJ</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Urol</span>
|
||
2016 Jan;26(1):11-6.
|
||
doi: 10.1097/MOU.0000000000000243.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26555692" target="_blank">26555692</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25973452">Clinical Inquiry: Does primary nocturnal enuresis affect childrens' self-esteem?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Phung P,
|
||
Kelsberg G,
|
||
Safranek S</span><br />
|
||
<span class="medgenPMjournal">J Fam Pract</span>
|
||
2015 Apr;64(4):250-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25973452" target="_blank">25973452</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21477399">Nocturnal enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kiddoo D</span><br />
|
||
<span class="medgenPMjournal">BMJ Clin Evid</span>
|
||
2011 Jan 31;2011
|
||
<span class="bold">PMID: </span><a href="/pubmed/21477399" target="_blank">21477399</a><a href="/pmc/articles/PMC3275307" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19450363">Nocturnal enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kiddoo D</span><br />
|
||
<span class="medgenPMjournal">BMJ Clin Evid</span>
|
||
2007 Oct 1;2007
|
||
<span class="bold">PMID: </span><a href="/pubmed/19450363" target="_blank">19450363</a><a href="/pmc/articles/PMC2943787" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Enuresis%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 (859)</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/34392083">An association between incontinence and antipsychotic drugs: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Arasteh A,
|
||
Mostafavi S,
|
||
Zununi Vahed S,
|
||
Mostafavi Montazeri SS</span><br />
|
||
<span class="medgenPMjournal">Biomed Pharmacother</span>
|
||
2021 Oct;142:112027.
|
||
Epub 2021 Aug 12
|
||
doi: 10.1016/j.biopha.2021.112027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34392083" target="_blank">34392083</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32053609">The association between allergic rhinitis and sleep: A systematic review and meta-analysis of observational studies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu J,
|
||
Zhang X,
|
||
Zhao Y,
|
||
Wang Y</span><br />
|
||
<span class="medgenPMjournal">PLoS One</span>
|
||
2020;15(2):e0228533.
|
||
Epub 2020 Feb 13
|
||
doi: 10.1371/journal.pone.0228533.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32053609" target="_blank">32053609</a><a href="/pmc/articles/PMC7018032" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30866915">Manual therapy for the pediatric population: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Parnell Prevost C,
|
||
Gleberzon B,
|
||
Carleo B,
|
||
Anderson K,
|
||
Cark M,
|
||
Pohlman KA</span><br />
|
||
<span class="medgenPMjournal">BMC Complement Altern Med</span>
|
||
2019 Mar 13;19(1):60.
|
||
doi: 10.1186/s12906-019-2447-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30866915" target="_blank">30866915</a><a href="/pmc/articles/PMC6417069" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21477399">Nocturnal enuresis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kiddoo D</span><br />
|
||
<span class="medgenPMjournal">BMJ Clin Evid</span>
|
||
2011 Jan 31;2011
|
||
<span class="bold">PMID: </span><a href="/pubmed/21477399" target="_blank">21477399</a><a href="/pmc/articles/PMC3275307" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16202382">What is the best treatment for nocturnal enuresis in children?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lyon C,
|
||
Schnall J</span><br />
|
||
<span class="medgenPMjournal">J Fam Pract</span>
|
||
2005 Oct;54(10):905-6, 909.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16202382" target="_blank">16202382</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Enuresis%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 (79)</a></div></div>
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