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<!--
UID=2649
ConceptID=C0005586
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Bipolar affective disorder<span class="h1sub">(BPAD)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>2649</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.">C0005586</a></dd><dt><span class="dotprefix"></span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
<td>Bipolar disorder</td></tr>
<tr><td><span class="bold">SNOMED CT: </span></td>
<td>Manic-depressive psychosis (13746004); Manic-depressive illness (13746004); MDI - Manic-depressive illness (13746004); Bipolar disorder (13746004); Bipolar affective disorder (13746004)</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:0007302">HP:0007302</a></td></tr>
<tr><td>Monarch Initiative:</td>
<td><a href="https://monarchinitiative.org/disease/MONDO:0004985" target="_blank">MONDO:0004985</a></td></tr>
<tr><td>OMIM<span class="superscript">®</span>:</td>
<td><a href="https://omim.org/entry/611535" target="_blank">611535</a></td></tr>
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<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">Bipolar disorder is an illness of mood characterized by alternating episodes of elevated and depressed moods, which are interspersed with euthymic periods. [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 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="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0005586[DISCUI]&amp;test_type=Clinical&amp;redirect=true" ref="ncbi_uid=2649">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=2649" target="_blank" href="/omim/611535">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=2649" ref="ncbi_uid=2649">V</a></span></span><span class="TLline">Bipolar affective disorder</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/21047" ref="tree=MeSH" title="MedGen record for Pathological Conditions, Signs and Symptoms">Pathological Conditions, Signs and Symptoms</a></span><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/14047" ref="tree=MeSH" title="MedGen record for Mental disorder">Mental disorder</a></span><ul><li><span class="TLline"><a href="/medgen/875788" ref="tree=MeSH" title="MedGen record for Bipolar and Related Disorders">Bipolar and Related Disorders</a></span><ul><li><span class="matched_ds">Bipolar affective disorder</span><ul><li><span class="TLline"><a href="/medgen/585" ref="tree=MeSH" title="MedGen record for Bipolar depression">Bipolar depression</a></span></li><li><span class="TLline"><a href="/medgen/7460" ref="tree=MeSH" title="MedGen record for Manic bipolar affective disorder">Manic bipolar affective disorder</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
</div>
<div class="portlet mgSection" id="ID_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_4297"><div><strong>DiGeorge syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>4297</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.">C0012236</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families. The major clinical manifestations of 22q11.2DS include congenital heart disease, particularly conotruncal malformations (ventricular septal defect, tetralogy of Fallot, interrupted aortic arch, and truncus arteriosus), palatal abnormalities (velopharyngeal incompetence, submucosal cleft palate, bifid uvula, and cleft palate), immune deficiency, characteristic facial features, and learning difficulties. Hearing loss can be sensorineural and/or conductive. Laryngotracheoesophageal, gastrointestinal, ophthalmologic, central nervous system, skeletal, and genitourinary anomalies also occur. Psychiatric illness and autoimmune disorders are more common in individuals with 22q11.2DS.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/4297">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_5956"><div><strong>Keratosis follicularis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>5956</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.">C0022595</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Darier-White disease (DAR), also known as keratosis follicularis, is an autosomal dominant skin disorder characterized by warty papules and plaques in seborrheic areas (central trunk, flexures, scalp, and forehead), palmoplantar pits, and distinctive nail abnormalities (Sakuntabhai et al., 1999). Onset is usually before the third decade, and penetrance is complete in adults, although expressivity is variable. Involvement may be severe, with widespread itchy malodorous crusted plaques, painful erosions, blistering, and mucosal lesions. Secondary infection is common. Sun, heat, and sweating exacerbate the symptoms. Darier disease never remits, but oral retinoids may reduce hyperkeratosis. Neuropsychiatric abnormalities, including mild mental retardation and epilepsy, have been described in association with Darier disease in a few families (Burge and Wilkinson, 1992); whether this is an association based on pleiotropism of the mutant gene or reflects coincidence is not clear. Histologic findings are (1) mild nonspecific perivascular infiltration in the dermis; (2) dermal villi protruding into the epidermis; (3) suprabasal detachment of the spinal layer leading to the formation of lacunae containing acantholytic cells; (4) in the more superficial epidermis, dyskeratotic round epidermal cells ('corps ronds'), the most distinctive feature; and (5) in the stratum corneum, 'grains' that resemble parakeratotic cells embedded in a hyperkeratotic horny layer. Electron microscopy reveals loss of desmosomal attachments, perinuclear aggregations of keratin filaments, and cytoplasmic vacuolization. Ultrastructural and immunologic studies suggest the disease results from an abnormality in the desmosome-keratin filament complex leading to a breakdown in cell adhesion.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/5956">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_208639"><div><strong>Kleefstra syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>208639</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:">C0795833</span></a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Kleefstra syndrome is characterized by intellectual disability, autistic-like features, childhood hypotonia, and distinctive facial features. The majority of individuals function in the moderate-to-severe spectrum of intellectual disability although a few individuals have mild delay and total IQ within low-normal range. While most have severe expressive speech delay with little speech development, general language development is usually at a higher level, making nonverbal communication possible. A complex pattern of other findings can also be observed; these include heart defects, renal/urologic defects, genital defects in males, severe respiratory infections, epilepsy / febrile seizures, psychiatric disorders, and extreme apathy or catatonic-like features after puberty.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/208639">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_163201"><div><strong>Gomez Lopez Hernandez syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>163201</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.">C0795959</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Gomez-Lopez-Hernandez syndrome (GLHS), also known as cerebellotrigeminal dermal dysplasia, is a rare neurocutaneous syndrome classically characterized by the triad of rhombencephalosynapsis, trigeminal anesthesia, often giving rise to corneal opacities, and bilateral parietal or parietooccipital alopecia. However, trigeminal anesthesia is an inconsistent finding (summary by Sukhudyan et al., 2010).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/163201">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_923000"><div><strong>Intellectual disability, X-linked 49</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>923000</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.">C0796221</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">CLCN4-related neurodevelopmental disorder (CLCN4-NDD), an X-linked disorder, is characterized in the 36 males reported to date by developmental delay or intellectual disability, behavioral/mental health issues (e.g., autism spectrum disorder, anxiety, hyperactivity, and bipolar disorder), epilepsy, and gastrointestinal dysfunction. The five heterozygous females with a de novo CLCN4 variant reported to date had findings very similar to those of affected males. Twenty-two of 25 heterozygous females identified in family studies following identification of an affected male were unaffected or had only mild specific learning difficulties and/or mental health concerns, whereas three were more severely affected.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/923000">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_331956"><div><strong>Lithium transport</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331956</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.">C1835356</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove nowrap">See: <a href="/medgen/331956">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_326975"><div><strong>Major affective disorder 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>326975</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.">C1839839</a></dd><dt><span class="dotprefix"></span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
<div class="spaceAbove nowrap">See: <a href="/medgen/326975">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_767235"><div><strong>Basal ganglia calcification, idiopathic, 4</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>767235</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.">C3554321</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Primary familial brain calcification (PFBC) is a neurodegenerative disorder with characteristic calcium deposits in the basal ganglia and other brain areas visualized on neuroimaging. Most affected individuals are in good health during childhood and young adulthood and typically present in the fourth to fifth decade with a gradually progressive movement disorder and neuropsychiatric symptoms. The movement disorder first manifests as clumsiness, fatigability, unsteady gait, slow or slurred speech, dysphagia, involuntary movements, or muscle cramping. Neuropsychiatric symptoms, often the first or most prominent manifestations, range from mild difficulty with concentration and memory to changes in personality and/or behavior, to psychosis and dementia. Seizures of various types occur frequently, some individuals experience chronic headache and vertigo; urinary urgency or incontinence may be present.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/767235">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_816174"><div><strong>Chromosome 22q13 duplication syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816174</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.">C3809844</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove nowrap">See: <a href="/medgen/816174">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1613937"><div><strong>Schizophrenia 19</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1613937</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.">C4539944</a></dd><dt><span class="dotprefix"></span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1613937">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1719546"><div><strong>Lissencephaly 10</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1719546</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.">C5394354</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Lissencephaly-10 (LIS10) is a neurologic disorder characterized by variably delayed development with mildly to moderately impaired intellectual development and language delay, as well as seizures, which are often intractable. There is a spectrum of severity, with some patients having normal early development and only borderline to mild cognitive impairment. Brain imaging shows features consistent with neuronal migration defects, including posterior-predominant lissencephaly, pachygyria, agyria, and subcortical band heterotopia (summary by Tsai et al., 2020).&#13; For a general description and a discussion of genetic heterogeneity of lissencephaly, see LIS1 (607432).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1719546">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1785079"><div><strong>Dystonia 30</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1785079</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.">C5543312</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Dystonia-30 (DYT30) is an autosomal dominant neurologic disorder characterized by the onset of symptoms in the first decades of life. Patients present with oromandibular, cervical, bulbar, or upper limb dystonia, and usually show slow progression to generalized dystonia. Some patients may lose ambulation. A subset of patients may also have neurocognitive impairment, including mild intellectual disability or psychiatric manifestations (summary by Steel et al., 2020).&#13; In a review of the pathogenesis of disorders with prominent dystonia, Monfrini et al. (2021) classified DYT30 as belonging to a group of neurologic disorders termed 'HOPS-associated neurologic disorders' (HOPSANDs), which are caused by mutations in genes encoding various components of the autophagic/endolysosomal system, including VPS16.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1785079">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1805690"><div><strong>Intellectual developmental disorder, autosomal dominant 67</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1805690</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.">C5677006</a></dd><dt><span class="dotprefix"></span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
<div class="spaceAbove">Autosomal dominant intellectual developmental disorder-67 (MRD67) is characterized by global developmental delay with variably impaired intellectual development apparent from infancy or early childhood. Additional features may include behavioral abnormalities, such as autism spectrum disorder (ASD) and ADHD, as well as language and sleeping difficulties. Brain imaging is normal (Ismail et al., 2022).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1805690">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1854654"><div><strong>Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1854654</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.">C5935628</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">ReNU syndrome (RENU), also known as neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language (NEDHAFA), is characterized by hypotonia, global developmental delay, severely impaired intellectual development with poor or absent speech, delayed walking or inability to walk, feeding difficulties with poor overall growth, seizures (in most), dysmorphic facial features, and brain anomalies, including ventriculomegaly, thin corpus callosum, and progressive white matter loss (Greene et al., 2024; Schot et al., 2024; Chen et al., 2024).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1854654">Condition Record</a></div></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_767235" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Basal ganglia calcification, idiopathic, 4</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816174" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 22q13 duplication syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_4297" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">DiGeorge syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1785079" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Dystonia 30</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_163201" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Gomez Lopez Hernandez syndrome</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (14)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1805690" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder, autosomal dominant 67</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_923000" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, X-linked 49</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_5956" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Keratosis follicularis</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_208639" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Kleefstra syndrome 1</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1719546" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lissencephaly 10</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_331956" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lithium transport</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_326975" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Major affective disorder 2</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1854654" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1613937" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Schizophrenia 19</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/34596304">Treatment resistance in bipolar affective disorder with recurrent mania course-Role of periventricular leukomalacia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Mamtani H,
Shiva L,
Nanjundaswamy MH,
Kamble N,
Prasad C,
Desai G,
Chandra PS,
Thippeswamy H</span><br />
<span class="medgenPMjournal">Bipolar Disord</span>
2022 Feb;24(1):93-96.
Epub 2021 Oct 13
doi: 10.1111/bdi.13138.
<span class="bold">PMID: </span><a href="/pubmed/34596304" target="_blank">34596304</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34257409">Treatment resistance in psychiatry: state of the art and new directions.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Howes OD,
Thase ME,
Pillinger T</span><br />
<span class="medgenPMjournal">Mol Psychiatry</span>
2022 Jan;27(1):58-72.
Epub 2021 Jul 13
doi: 10.1038/s41380-021-01200-3.
<span class="bold">PMID: </span><a href="/pubmed/34257409" target="_blank">34257409</a><a href="/pmc/articles/PMC8960394" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32447355">Clinical picture and treatment of bipolar affective disorder in children and adolescents.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cichoń L,
Janas-Kozik M,
Siwiec A,
Rybakowski JK</span><br />
<span class="medgenPMjournal">Psychiatr Pol</span>
2020 Mar 29;54(1):35-50.
doi: 10.12740/PP/OnlineFirst/92740.
<span class="bold">PMID: </span><a href="/pubmed/32447355" target="_blank">32447355</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22bipolar%20affective%20disorder%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 (105)</a></div><h3 class="subhead">Curated<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpCurated"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3><h3 class="nl vspace"><a href="https://www.nice.org.uk/guidance/cg185" target="_blank">UK NICE Clinical Guideline CG185, Bipolar disorder: assessment and management, 2023</a></h3>
<h3 class="nl vspace"><a href="https://www.nice.org.uk/guidance/cg192" target="_blank">UK NICE Clinical Guideline CG192, Antenatal and postnatal mental health: clinical management and service guidance, 2020</a></h3>
</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/37098202">Ketogenic diet in therapy of bipolar affective disorder - case report and literature review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Chmiel I</span><br />
<span class="medgenPMjournal">Psychiatr Pol</span>
2022 Dec 31;56(6):1345-1363.
doi: 10.12740/PP/OnlineFirst/136356.
<span class="bold">PMID: </span><a href="/pubmed/37098202" target="_blank">37098202</a></div>
<div class="nl"><a target="_blank" href="/pubmed/15338640">Genetics of schizophrenia and bipolar affective disorder: strategies to identify candidate genes.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Porteous DJ,
Evans KL,
Millar JK,
Pickard BS,
Thomson PA,
James R,
MacGregor S,
Wray NR,
Visscher PM,
Muir WJ,
Blackwood DH</span><br />
<span class="medgenPMjournal">Cold Spring Harb Symp Quant Biol</span>
2003;68:383-94.
doi: 10.1101/sqb.2003.68.383.
<span class="bold">PMID: </span><a href="/pubmed/15338640" target="_blank">15338640</a></div>
<div class="nl"><a target="_blank" href="/pubmed/7766338">Drug-induced mania.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Peet M,
Peters S</span><br />
<span class="medgenPMjournal">Drug Saf</span>
1995 Feb;12(2):146-53.
doi: 10.2165/00002018-199512020-00007.
<span class="bold">PMID: </span><a href="/pubmed/7766338" target="_blank">7766338</a></div>
<div class="nl"><a target="_blank" href="/pubmed/3076673">Aging and mania.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Rubin EH</span><br />
<span class="medgenPMjournal">Psychiatr Dev</span>
1988 Winter;6(4):329-37.
<span class="bold">PMID: </span><a href="/pubmed/3076673" target="_blank">3076673</a></div>
<div class="nl"><a target="_blank" href="/pubmed/534810">Postpartum mania.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kadrmas A,
Winokur G,
Crowe R</span><br />
<span class="medgenPMjournal">Br J Psychiatry</span>
1979 Dec;135:551-4.
doi: 10.1192/bjp.135.6.551.
<span class="bold">PMID: </span><a href="/pubmed/534810" target="_blank">534810</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bipolar%20affective%20disorder%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 (873)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/35342202">Antipsychotic-Induced Laryngeal Dystonia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">O'Neill JR,
Stephenson C</span><br />
<span class="medgenPMjournal">Psychopharmacol Bull</span>
2022 Feb 25;52(1):61-67.
<span class="bold">PMID: </span><a href="/pubmed/35342202" target="_blank">35342202</a><a href="/pmc/articles/PMC8896750" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31727221">Frontotemporal dementia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Miller B,
Llibre Guerra JJ</span><br />
<span class="medgenPMjournal">Handb Clin Neurol</span>
2019;165:33-45.
doi: 10.1016/B978-0-444-64012-3.00003-4.
<span class="bold">PMID: </span><a href="/pubmed/31727221" target="_blank">31727221</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6581756">Seasonal affective disorder. A description of the syndrome and preliminary findings with light therapy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Rosenthal NE,
Sack DA,
Gillin JC,
Lewy AJ,
Goodwin FK,
Davenport Y,
Mueller PS,
Newsome DA,
Wehr TA</span><br />
<span class="medgenPMjournal">Arch Gen Psychiatry</span>
1984 Jan;41(1):72-80.
doi: 10.1001/archpsyc.1984.01790120076010.
<span class="bold">PMID: </span><a href="/pubmed/6581756" target="_blank">6581756</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6750043">Schizoaffective disorders.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Clayton PJ</span><br />
<span class="medgenPMjournal">J Nerv Ment Dis</span>
1982 Nov;170(11):646-50.
doi: 10.1097/00005053-198211000-00002.
<span class="bold">PMID: </span><a href="/pubmed/6750043" target="_blank">6750043</a></div>
<div class="nl"><a target="_blank" href="/pubmed/4412212">Bipolar affective disorder and alcoholism.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Morrison JR</span><br />
<span class="medgenPMjournal">Am J Psychiatry</span>
1974 Oct;131(10):1130-3.
doi: 10.1176/ajp.131.10.1130.
<span class="bold">PMID: </span><a href="/pubmed/4412212" target="_blank">4412212</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bipolar%20affective%20disorder%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 (810)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/37098202">Ketogenic diet in therapy of bipolar affective disorder - case report and literature review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Chmiel I</span><br />
<span class="medgenPMjournal">Psychiatr Pol</span>
2022 Dec 31;56(6):1345-1363.
doi: 10.12740/PP/OnlineFirst/136356.
<span class="bold">PMID: </span><a href="/pubmed/37098202" target="_blank">37098202</a></div>
<div class="nl"><a target="_blank" href="/pubmed/36427216">Weak legs.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Timmons P,
Williamson A,
Gibbs V,
Torgersen A</span><br />
<span class="medgenPMjournal">Acute Med</span>
2022;21(3):153-156.
doi: 10.52964/AMJA.0917.
<span class="bold">PMID: </span><a href="/pubmed/36427216" target="_blank">36427216</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32447355">Clinical picture and treatment of bipolar affective disorder in children and adolescents.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cichoń L,
Janas-Kozik M,
Siwiec A,
Rybakowski JK</span><br />
<span class="medgenPMjournal">Psychiatr Pol</span>
2020 Mar 29;54(1):35-50.
doi: 10.12740/PP/OnlineFirst/92740.
<span class="bold">PMID: </span><a href="/pubmed/32447355" target="_blank">32447355</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31727221">Frontotemporal dementia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Miller B,
Llibre Guerra JJ</span><br />
<span class="medgenPMjournal">Handb Clin Neurol</span>
2019;165:33-45.
doi: 10.1016/B978-0-444-64012-3.00003-4.
<span class="bold">PMID: </span><a href="/pubmed/31727221" target="_blank">31727221</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27516079">Lithium Poisoning.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Baird-Gunning J,
Lea-Henry T,
Hoegberg LCG,
Gosselin S,
Roberts DM</span><br />
<span class="medgenPMjournal">J Intensive Care Med</span>
2017 May;32(4):249-263.
Epub 2016 Aug 11
doi: 10.1177/0885066616651582.
<span class="bold">PMID: </span><a href="/pubmed/27516079" target="_blank">27516079</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bipolar%20affective%20disorder%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 (564)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/36696101">Lipid Alteration Signature in the Blood Plasma of Individuals With Schizophrenia, Depression, and Bipolar Disorder.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tkachev A,
Stekolshchikova E,
Vanyushkina A,
Zhang H,
Morozova A,
Zozulya S,
Kurochkin I,
Anikanov N,
Egorova A,
Yushina E,
Vogl T,
Senner F,
Schaupp SK,
Reich-Erkelenz D,
Papiol S,
Kohshour MO,
Klöhn-Saghatolislam F,
Kalman JL,
Heilbronner U,
Heilbronner M,
Gade K,
Comes AL,
Budde M,
Anderson-Schmidt H,
Adorjan K,
Wiltfang J,
Reininghaus EZ,
Juckel G,
Dannlowski U,
Fallgatter A,
Spitzer C,
Schmauß M,
von Hagen M,
Zorkina Y,
Reznik A,
Barkhatova A,
Lisov R,
Mokrov N,
Panov M,
Zubkov D,
Petrova D,
Zhou C,
Liu Y,
Pu J,
Falkai P,
Kostyuk G,
Klyushnik T,
Schulze TG,
Xie P,
Schulte EC,
Khaitovich P</span><br />
<span class="medgenPMjournal">JAMA Psychiatry</span>
2023 Mar 1;80(3):250-259.
doi: 10.1001/jamapsychiatry.2022.4350.
<span class="bold">PMID: </span><a href="/pubmed/36696101" target="_blank">36696101</a><a href="/pmc/articles/PMC9878436" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34596304">Treatment resistance in bipolar affective disorder with recurrent mania course-Role of periventricular leukomalacia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Mamtani H,
Shiva L,
Nanjundaswamy MH,
Kamble N,
Prasad C,
Desai G,
Chandra PS,
Thippeswamy H</span><br />
<span class="medgenPMjournal">Bipolar Disord</span>
2022 Feb;24(1):93-96.
Epub 2021 Oct 13
doi: 10.1111/bdi.13138.
<span class="bold">PMID: </span><a href="/pubmed/34596304" target="_blank">34596304</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32447355">Clinical picture and treatment of bipolar affective disorder in children and adolescents.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cichoń L,
Janas-Kozik M,
Siwiec A,
Rybakowski JK</span><br />
<span class="medgenPMjournal">Psychiatr Pol</span>
2020 Mar 29;54(1):35-50.
doi: 10.12740/PP/OnlineFirst/92740.
<span class="bold">PMID: </span><a href="/pubmed/32447355" target="_blank">32447355</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6750043">Schizoaffective disorders.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Clayton PJ</span><br />
<span class="medgenPMjournal">J Nerv Ment Dis</span>
1982 Nov;170(11):646-50.
doi: 10.1097/00005053-198211000-00002.
<span class="bold">PMID: </span><a href="/pubmed/6750043" target="_blank">6750043</a></div>
<div class="nl"><a target="_blank" href="/pubmed/534810">Postpartum mania.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kadrmas A,
Winokur G,
Crowe R</span><br />
<span class="medgenPMjournal">Br J Psychiatry</span>
1979 Dec;135:551-4.
doi: 10.1192/bjp.135.6.551.
<span class="bold">PMID: </span><a href="/pubmed/534810" target="_blank">534810</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bipolar%20affective%20disorder%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 (363)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/38359838">Psilocybin-assisted psychotherapy for treatment resistant depression: A randomized clinical trial evaluating repeated doses of psilocybin.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Rosenblat JD,
Meshkat S,
Doyle Z,
Kaczmarek E,
Brudner RM,
Kratiuk K,
Mansur RB,
Schulz-Quach C,
Sethi R,
Abate A,
Ali S,
Bawks J,
Blainey MG,
Brietzke E,
Cronin V,
Danilewitz J,
Dhawan S,
Di Fonzo A,
Di Fonzo M,
Drzadzewski P,
Dunlop W,
Fiszter H,
Gomes FA,
Grewal S,
Leon-Carlyle M,
McCallum M,
Mofidi N,
Offman H,
Riva-Cambrin J,
Schmidt J,
Smolkin M,
Quinn JM,
Zumrova A,
Marlborough M,
McIntyre RS</span><br />
<span class="medgenPMjournal">Med</span>
2024 Mar 8;5(3):190-200.e5.
Epub 2024 Feb 14
doi: 10.1016/j.medj.2024.01.005.
<span class="bold">PMID: </span><a href="/pubmed/38359838" target="_blank">38359838</a></div>
<div class="nl"><a target="_blank" href="/pubmed/38056909">IMPA1 dependent regulation of phosphatidylinositol 4,5-bisphosphate and calcium signalling by lithium.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Saha S,
Krishnan H,
Raghu P</span><br />
<span class="medgenPMjournal">Life Sci Alliance</span>
2024 Feb;7(2)
Epub 2023 Dec 6
doi: 10.26508/lsa.202302425.
<span class="bold">PMID: </span><a href="/pubmed/38056909" target="_blank">38056909</a><a href="/pmc/articles/PMC10700560" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34952447">Serum glial cell derived neurotrophic factor (GDNF) as a predictor of response to HD-tDCS in bipolar affective disorder.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Veenakumari M,
Goyal N,
Kumar M,
Kshitiz KK,
Kumar P</span><br />
<span class="medgenPMjournal">Asian J Psychiatr</span>
2022 Feb;68:102965.
Epub 2021 Dec 16
doi: 10.1016/j.ajp.2021.102965.
<span class="bold">PMID: </span><a href="/pubmed/34952447" target="_blank">34952447</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26899842">Efficiency of Umbilical Cord Blood Cells in Patients with Treatment-Resistant Depressions.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Smulevich AB,
Dubnitskaya EB,
Voronova EI,
Morozova YV,
Radaev SM</span><br />
<span class="medgenPMjournal">Bull Exp Biol Med</span>
2016 Feb;160(4):583-8.
Epub 2016 Feb 22
doi: 10.1007/s10517-016-3222-8.
<span class="bold">PMID: </span><a href="/pubmed/26899842" target="_blank">26899842</a><a href="/pmc/articles/PMC7087609" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/7840347">Unstable genes--unstable mind?</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Petronis A,
Kennedy JL</span><br />
<span class="medgenPMjournal">Am J Psychiatry</span>
1995 Feb;152(2):164-72.
doi: 10.1176/ajp.152.2.164.
<span class="bold">PMID: </span><a href="/pubmed/7840347" target="_blank">7840347</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bipolar%20affective%20disorder%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 (549)</a></div></div>
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<div class="nl"><a target="_blank" href="/pubmed/28472082">Efficacy of cognitive-behavioral therapy in patients with bipolar disorder: A meta-analysis of randomized controlled trials.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Chiang KJ,
Tsai JC,
Liu D,
Lin CH,
Chiu HL,
Chou KR</span><br />
<span class="medgenPMjournal">PLoS One</span>
2017;12(5):e0176849.
Epub 2017 May 4
doi: 10.1371/journal.pone.0176849.
<span class="bold">PMID: </span><a href="/pubmed/28472082" target="_blank">28472082</a><a href="/pmc/articles/PMC5417606" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27758835">Relationship between childhood adversity and bipolar affective disorder: systematic review and meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Palmier-Claus JE,
Berry K,
Bucci S,
Mansell W,
Varese F</span><br />
<span class="medgenPMjournal">Br J Psychiatry</span>
2016 Dec;209(6):454-459.
Epub 2016 Oct 6
doi: 10.1192/bjp.bp.115.179655.
<span class="bold">PMID: </span><a href="/pubmed/27758835" target="_blank">27758835</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26969211">Biological aspects and candidate biomarkers for psychotic bipolar disorder: A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Buoli M,
Caldiroli A,
Cumerlato Melter C,
Serati M,
de Nijs J,
Altamura AC</span><br />
<span class="medgenPMjournal">Psychiatry Clin Neurosci</span>
2016 Jun;70(6):227-44.
Epub 2016 Apr 28
doi: 10.1111/pcn.12386.
<span class="bold">PMID: </span><a href="/pubmed/26969211" target="_blank">26969211</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25735195">A systematic review and meta-analysis of premature mortality in bipolar affective disorder.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hayes JF,
Miles J,
Walters K,
King M,
Osborn DP</span><br />
<span class="medgenPMjournal">Acta Psychiatr Scand</span>
2015 Jun;131(6):417-25.
Epub 2015 Mar 3
doi: 10.1111/acps.12408.
<span class="bold">PMID: </span><a href="/pubmed/25735195" target="_blank">25735195</a><a href="/pmc/articles/PMC4939858" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25662294">Neurobiological and behavioural studies of affective instability in clinical populations: a systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Broome MR,
He Z,
Iftikhar M,
Eyden J,
Marwaha S</span><br />
<span class="medgenPMjournal">Neurosci Biobehav Rev</span>
2015 Apr;51:243-54.
Epub 2015 Feb 4
doi: 10.1016/j.neubiorev.2015.01.021.
<span class="bold">PMID: </span><a href="/pubmed/25662294" target="_blank">25662294</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bipolar%20affective%20disorder%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 (37)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0005586%5bDISCUI%5d&amp;filter=method%3A2%5F19" target="_blank">Targeted variant analysis (1)</a></li>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Bipolar%20affective%20disorder" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22bipolar%20affective%20disorder%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">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><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Bipolar%20affective%20disorder%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. 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><h3 class="subhead">Curated</h3><ul class="a_poppers"><li><a target="_blank" href="https://www.nice.org.uk/guidance/cg185">NICE, 2023</a><div>UK NICE Clinical Guideline CG185, Bipolar disorder: assessment and management, 2023</div></li><li><a target="_blank" href="https://www.nice.org.uk/guidance/cg192">NICE, 2020</a><div>UK NICE Clinical Guideline CG192, Antenatal and postnatal mental health: clinical management and service guidance, 2020</div></li></ul></div>
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