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<!--
|
||
UID=102359
|
||
ConceptID=C0158779
|
||
-->
|
||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Cervical rib</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>102359</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.">C0158779</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Cervical rib disease; Cervical ribs</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Cervical rib (72535009); Supernumerary rib in cervical region (72535009); Cervical rib (1285171005)</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:0000891">HP:0000891</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0007303" target="_blank">MONDO:0007303</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/117900" target="_blank">117900</a></td></tr>
|
||
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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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">Presence of rib formation in the cervical region. [from <a title="NCI Thesaurus" href="http://ncit.nci.nih.gov" class="defSource" target="_blank">NCI</a>]</div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_102">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_105425"><div><strong>Abnormality of the nervous system</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>105425</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.">C0497552</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An abnormality of the nervous system.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/105425">Feature record</a> | <a href="/medgen?term=%22Abnormality%20of%20the%20nervous%20system%22%5BClinical%20Features%5D%20OR%20105425%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_102359"><div><strong>Cervical rib</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>102359</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.">C0158779</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Presence of rib formation in the cervical region.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/102359">Feature record</a> | <a href="/medgen?term=%22Cervical%20rib%22%5BClinical%20Features%5D%20OR%20102359%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of the musculoskeletal system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_102359" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cervical rib</a></span></li></ul></li><li><span class="TLline">Abnormality of the nervous system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_105425" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Abnormality of the nervous system</a></span></li></ul></li></ul></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_118">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=102359" target="_blank" href="/omim/117900">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Cervical rib</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/311052" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Disorder">Non-Neoplastic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/317955" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Disorder by Special Category">Non-Neoplastic Disorder by Special Category</a></span><ul><li><span class="TLline"><a href="/medgen/90143" ref="tree=MeSH" title="MedGen record for Deformity">Deformity</a></span><ul><li><span class="TLline"><a href="/medgen/83380" ref="tree=MeSH" title="MedGen record for Supernumerary ribs">Supernumerary ribs</a></span><ul><li><span class="matched_ds">Cervical rib</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_3486"><div><strong>Cleidocranial dysostosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>3486</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.">C0008928</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cleidocranial dysplasia (CCD) spectrum disorder is a skeletal dysplasia that represents a clinical continuum ranging from classic CCD (triad of delayed closure of the cranial sutures, hypoplastic or aplastic clavicles, and dental abnormalities), to mild CCD, to isolated dental anomalies without other skeletal features. Individuals with classic CCD spectrum disorder typically have abnormally large, wide-open fontanelles at birth that may remain open throughout life. Clavicular hypoplasia can result in narrow, sloping shoulders that can be opposed at the midline. Moderate short stature may be observed, with most affected individuals being shorter than their unaffected sibs. Dental anomalies may include delayed eruption of secondary dentition, failure to shed the primary teeth, and supernumerary teeth. Individuals with CCD spectrum disorder are at increased risk of developing recurrent sinus infections, recurrent ear infections leading to conductive hearing loss, and upper airway obstruction. Intelligence is typically normal.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/3486">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_102359"><div><strong>Cervical rib</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>102359</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.">C0158779</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Presence of rib formation in the cervical region.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/102359">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_61235"><div><strong>Radial aplasia-thrombocytopenia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>61235</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.">C0175703</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Thrombocytopenia absent radius (TAR) syndrome is characterized by bilateral absence of the radii with the presence of both thumbs, and thrombocytopenia that is generally transient. Thrombocytopenia may be congenital or may develop within the first few weeks to months of life; in general, thrombocytopenic episodes decrease with age. Cow's milk allergy is common and can be associated with exacerbation of thrombocytopenia. Other anomalies of the skeleton (upper and lower limbs, ribs, and vertebrae), heart, and genitourinary system (renal anomalies and agenesis of uterus, cervix, and upper part of the vagina) can occur.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/61235">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_66317"><div><strong>KBG syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>66317</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.">C0220687</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">KBG syndrome is typically characterized by macrodontia (especially of the upper central incisors), characteristic facial features (triangular face, brachycephaly, synophrys, widely spaced eyes, broad or bushy eyebrows, prominent ears, prominent nasal bridge, bulbous nose, anteverted nares, long philtrum, and thin vermilion of the upper lip), short stature, developmental delay / intellectual disability, and behavioral issues. Affected individuals may have feeding difficulties (particularly in infancy), skeletal anomalies (brachydactyly, large anterior fontanelle with delayed closure, scoliosis), hearing loss (conductive, mixed, and sensorineural), seizure disorder, and brain malformations. There is significant variability in the clinical findings, even between affected members of the same family.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/66317">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_120519"><div><strong>Nager syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>120519</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.">C0265245</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Nager syndrome is the prototype for a group of disorders collectively referred to as the acrofacial dysostoses (AFDs), which are characterized by malformation of the craniofacial skeleton and the limbs. The major facial features of Nager syndrome include downslanted palpebral fissures, midface retrusion, and micrognathia, the latter of which often requires the placement of a tracheostomy in early childhood. Limb defects typically involve the anterior (radial) elements of the upper limbs and manifest as small or absent thumbs, triphalangeal thumbs, radial hypoplasia or aplasia, and radioulnar synostosis. Phocomelia of the upper limbs and, occasionally, lower-limb defects have also been reported. The presence of anterior upper-limb defects and the typical lack of lower-limb involvement distinguishes Nager syndrome from Miller syndrome (263750), another rare AFD; however, distinguishing Nager syndrome from other AFDs, including Miller syndrome, can be challenging (summary by Bernier et al., 2012).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/120519">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_162917"><div><strong>Simpson-Golabi-Behmel syndrome type 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>162917</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.">C0796154</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Simpson-Golabi-Behmel syndrome type 1 (SGBS1) is characterized by pre- and postnatal macrosomia; distinctive craniofacial features (including macrocephaly, coarse facial features, macrostomia, macroglossia, and palate abnormalities); and, commonly, mild-to-severe intellectual disability with or without structural brain anomalies. Other variable findings include supernumerary nipples, diastasis recti / umbilical hernia, congenital heart defects, diaphragmatic hernia, genitourinary defects, and gastrointestinal issues. Skeletal anomalies can include vertebral fusion, scoliosis, rib anomalies, and congenital hip dislocation. Hand anomalies can include large hands and postaxial polydactyly. Affected individuals are at increased risk for embryonal tumors including Wilms tumor, hepatoblastoma, adrenal neuroblastoma, gonadoblastoma, hepatocellular carcinoma, and medulloblastoma.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/162917">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_318617"><div><strong>Cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>318617</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.">C1832391</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/318617">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_347608"><div><strong>Becker nevus syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347608</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.">C1858042</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Becker nevus (BN) is a cutaneous hamartoma affecting approximately 1 in 200 individuals that appears in childhood as a unilateral tan patch, and increases in thickness, pigmentation, and hair growth during adolescence. Histologically, epidermal acanthosis is accompanied by irregularly dispersed ectopic smooth muscle bundles and increased terminal hair follicles (summary by Cai et al., 2017). Becker nevus syndrome (BNS) is a phenotype characterized by the presence of a Becker nevus in association with unilateral hypoplasia of breast or other cutaneous, muscular, or skeletal defects (Happle and Koopman, 1997).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347608">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_351216"><div><strong>Short stature and Facioauriculothoracic malformations</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>351216</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.">C1864791</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/351216">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_400936"><div><strong>Acroosteolysis-keloid-like lesions-premature aging syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>400936</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.">C1866182</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Penttinen syndrome (PENTT) is characterized by a prematurely aged appearance involving lipoatrophy and epidermal and dermal atrophy, as well as hypertrophic lesions that resemble scars, thin hair, proptosis, underdeveloped cheekbones, and marked acroosteolysis (Johnston et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/400936">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_444022"><div><strong>Pancreatic hypoplasia-diabetes-congenital heart disease syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>444022</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.">C2931296</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">This syndrome has characteristics of partial pancreatic agenesis, diabetes mellitus, and heart anomalies (including transposition of the great vessels, ventricular or atrial septal defects, pulmonary stenosis, or patent ductus arteriosis). It has been described in one Japanese family, in which the mother and at least two of her four children were affected (another two children died shortly after birth). The syndrome appears to be inherited as an autosomal dominant trait.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/444022">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_501171"><div><strong>Craniofacial microsomia 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>501171</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.">C3495417</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Craniofacial microsomia is a term used to describe a spectrum of abnormalities that primarily affect the development of the skull (cranium) and face before birth. Microsomia means abnormal smallness of body structures. Most people with craniofacial microsomia have differences in the size and shape of facial structures between the right and left sides of the face (facial asymmetry). In about two-thirds of cases, both sides of the face have abnormalities, which usually differ from one side to the other. Other individuals with craniofacial microsomia are affected on only one side of the face. The facial characteristics in craniofacial microsomia typically include underdevelopment of one side of the upper or lower jaw (maxillary or mandibular hypoplasia), which can cause dental problems and difficulties with feeding and speech. In cases of severe mandibular hypoplasia, breathing may also be affected.\n\nPeople with craniofacial microsomia usually have ear abnormalities affecting one or both ears, typically to different degrees. They may have growths of skin (skin tags) in front of the ear (preauricular tags), an underdeveloped or absent external ear (microtia or anotia), or a closed or absent ear canal; these abnormalities may lead to hearing loss. Eye problems are less common in craniofacial microsomia, but some affected individuals have an unusually small eyeball (microphthalmia) or other eye abnormalities that result in vision loss.\n\nAbnormalities in other parts of the body, such as malformed bones of the spine (vertebrae), abnormally shaped kidneys, and heart defects, may also occur in people with craniofacial microsomia.\n\nMany other terms have been used for craniofacial microsomia. These other names generally refer to forms of craniofacial microsomia with specific combinations of signs and symptoms, although sometimes they are used interchangeably. Hemifacial microsomia often refers to craniofacial microsomia with maxillary or mandibular hypoplasia. People with hemifacial microsomia and noncancerous (benign) growths in the eye called epibulbar dermoids may be said to have Goldenhar syndrome or oculoauricular dysplasia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/501171">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934663"><div><strong>ZTTK syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934663</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.">C4310696</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">ZTTK syndrome (ZTTKS) is a severe multisystem developmental disorder characterized by delayed psychomotor development and intellectual disability. Affected individuals have characteristic dysmorphic facial features, hypotonia, poor feeding, poor overall growth, and eye or visual abnormalities. Most patients also have musculoskeletal abnormalities, and some have congenital defects of the heart and urogenital system. Brain imaging usually shows developmental abnormalities such as gyral changes, cortical and/or cerebellar atrophy, and thin corpus callosum (summary by Kim et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934663">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1779339"><div><strong>KINSSHIP syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1779339</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.">C5543317</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">KINSSHIP syndrome (KINS) is an autosomal dominant disorder characterized by a recognizable pattern of anomalies including developmental delay, impaired intellectual development, seizures, mesomelic dysplasia, dysmorphic facial features, horseshoe or hypoplastic kidney, and failure to thrive (summary by Voisin et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1779339">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1799326"><div><strong>Orofaciodigital syndrome 18</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1799326</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.">C5567903</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Orofaciodigital syndrome XVIII (OFD18) is characterized by short stature, brachymesophalangy, pre- and postaxial polysyndactyly, and stocky femoral necks, as well as oral anomalies and dysmorphic facial features (Thevenon et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1799326">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_400936" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acroosteolysis-keloid-like lesions-premature aging syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347608" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Becker nevus syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_102359" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cervical rib</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_318617" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_3486" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cleidocranial dysostosis</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (15)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_501171" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Craniofacial microsomia 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_66317" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">KBG syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1779339" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">KINSSHIP syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_120519" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nager syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1799326" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Orofaciodigital syndrome 18</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_444022" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pancreatic hypoplasia-diabetes-congenital heart disease syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_61235" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Radial aplasia-thrombocytopenia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_351216" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Short stature and Facioauriculothoracic malformations</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_162917" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Simpson-Golabi-Behmel syndrome type 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934663" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">ZTTK 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/36018621">Thoracic outlet syndrome: a review for the primary care provider.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cavanna AC,
|
||
Giovanis A,
|
||
Daley A,
|
||
Feminella R,
|
||
Chipman R,
|
||
Onyeukwu V</span><br />
|
||
<span class="medgenPMjournal">J Osteopath Med</span>
|
||
2022 Nov 1;122(11):587-599.
|
||
Epub 2022 Aug 29
|
||
doi: 10.1515/jom-2021-0276.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36018621" target="_blank">36018621</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30122304">Outcomes of Surgical Management of Neurogenic Thoracic Outlet Syndrome: A Systematic Review and Bayesian Perspective.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yin ZG,
|
||
Gong KT,
|
||
Zhang JB</span><br />
|
||
<span class="medgenPMjournal">J Hand Surg Am</span>
|
||
2019 May;44(5):416.e1-416.e17.
|
||
Epub 2018 Aug 16
|
||
doi: 10.1016/j.jhsa.2018.06.120.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30122304" target="_blank">30122304</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28189360">Clinical presentation and management of arterial thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vemuri C,
|
||
McLaughlin LN,
|
||
Abuirqeba AA,
|
||
Thompson RW</span><br />
|
||
<span class="medgenPMjournal">J Vasc Surg</span>
|
||
2017 May;65(5):1429-1439.
|
||
Epub 2017 Feb 8
|
||
doi: 10.1016/j.jvs.2016.11.039.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28189360" target="_blank">28189360</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22cervical%20rib%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 (15)</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/38704183">Thoracic outlet syndrome in women.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mulatti GC,
|
||
Dalio MB,
|
||
de Moraes TM,
|
||
Attie GA,
|
||
Brito-Queiroz A,
|
||
Joviliano EE</span><br />
|
||
<span class="medgenPMjournal">Semin Vasc Surg</span>
|
||
2024 Mar;37(1):44-49.
|
||
Epub 2024 Feb 2
|
||
doi: 10.1053/j.semvascsurg.2024.01.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38704183" target="_blank">38704183</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31859722">Thoracic outlet syndrome: a narrative review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Masocatto NO,
|
||
Da-Matta T,
|
||
Prozzo TG,
|
||
Couto WJ,
|
||
Porfirio G</span><br />
|
||
<span class="medgenPMjournal">Rev Col Bras Cir</span>
|
||
2019;46(5):e20192243.
|
||
Epub 2019 Dec 20
|
||
doi: 10.1590/0100-6991e-20192243.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31859722" target="_blank">31859722</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27975060">The Epidemiological, Morphological, and Clinical Aspects of the Cervical Ribs in Humans.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Spadliński Ł,
|
||
Cecot T,
|
||
Majos A,
|
||
Stefańczyk L,
|
||
Pietruszewska W,
|
||
Wysiadecki G,
|
||
Topol M,
|
||
Polguj M</span><br />
|
||
<span class="medgenPMjournal">Biomed Res Int</span>
|
||
2016;2016:8034613.
|
||
Epub 2016 Nov 15
|
||
doi: 10.1155/2016/8034613.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27975060" target="_blank">27975060</a><a href="/pmc/articles/PMC5126392" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22581530">The thoracic outlet syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ferrante MA</span><br />
|
||
<span class="medgenPMjournal">Muscle Nerve</span>
|
||
2012 Jun;45(6):780-95.
|
||
doi: 10.1002/mus.23235.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22581530" target="_blank">22581530</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14550762">A proposed inhalation reference concentration for methanol.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Starr TB,
|
||
Festa JL</span><br />
|
||
<span class="medgenPMjournal">Regul Toxicol Pharmacol</span>
|
||
2003 Oct;38(2):224-31.
|
||
doi: 10.1016/s0273-2300(03)00095-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14550762" target="_blank">14550762</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20rib%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 (138)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36018621">Thoracic outlet syndrome: a review for the primary care provider.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cavanna AC,
|
||
Giovanis A,
|
||
Daley A,
|
||
Feminella R,
|
||
Chipman R,
|
||
Onyeukwu V</span><br />
|
||
<span class="medgenPMjournal">J Osteopath Med</span>
|
||
2022 Nov 1;122(11):587-599.
|
||
Epub 2022 Aug 29
|
||
doi: 10.1515/jom-2021-0276.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36018621" target="_blank">36018621</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35963513">Thoracic outlet syndrome: a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Panther EJ,
|
||
Reintgen CD,
|
||
Cueto RJ,
|
||
Hao KA,
|
||
Chim H,
|
||
King JJ</span><br />
|
||
<span class="medgenPMjournal">J Shoulder Elbow Surg</span>
|
||
2022 Nov;31(11):e545-e561.
|
||
Epub 2022 Aug 10
|
||
doi: 10.1016/j.jse.2022.06.026.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35963513" target="_blank">35963513</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31859722">Thoracic outlet syndrome: a narrative review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Masocatto NO,
|
||
Da-Matta T,
|
||
Prozzo TG,
|
||
Couto WJ,
|
||
Porfirio G</span><br />
|
||
<span class="medgenPMjournal">Rev Col Bras Cir</span>
|
||
2019;46(5):e20192243.
|
||
Epub 2019 Dec 20
|
||
doi: 10.1590/0100-6991e-20192243.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31859722" target="_blank">31859722</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17826254">Diagnosis of thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sanders RJ,
|
||
Hammond SL,
|
||
Rao NM</span><br />
|
||
<span class="medgenPMjournal">J Vasc Surg</span>
|
||
2007 Sep;46(3):601-4.
|
||
doi: 10.1016/j.jvs.2007.04.050.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17826254" target="_blank">17826254</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14125251">CERVICAL RIB SYNDROME.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">WILKINS R</span><br />
|
||
<span class="medgenPMjournal">Manch Med Gaz</span>
|
||
1964;43:18-21.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14125251" target="_blank">14125251</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20rib%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 (209)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34775010">Role of Botulinum Toxin in Pectoralis Minor Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Martinez Del Carmen DT,
|
||
Martí Mestre FX,
|
||
Tripodi P,
|
||
Macia Vidueira I,
|
||
Ramos Izquierdo R,
|
||
Romera Villegas A</span><br />
|
||
<span class="medgenPMjournal">Ann Vasc Surg</span>
|
||
2022 Apr;81:225-231.
|
||
Epub 2021 Nov 11
|
||
doi: 10.1016/j.avsg.2021.09.032.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34775010" target="_blank">34775010</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26233638">A 64-year old woman with right hand swelling and paresthesia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kalchiem-Dekel O,
|
||
Davidesko S,
|
||
Maimon N</span><br />
|
||
<span class="medgenPMjournal">Eur J Intern Med</span>
|
||
2015 Dec;26(10):e59-60.
|
||
Epub 2015 Jul 29
|
||
doi: 10.1016/j.ejim.2015.07.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26233638" target="_blank">26233638</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25427003">Treatment for thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Povlsen B,
|
||
Hansson T,
|
||
Povlsen SD</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2014 Nov 26;2014(11):CD007218.
|
||
doi: 10.1002/14651858.CD007218.pub3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25427003" target="_blank">25427003</a><a href="/pmc/articles/PMC11245746" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24035686">Cervical rib resulting in amaurosis fugax and stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kalita J,
|
||
Kumar P,
|
||
Misra UK</span><br />
|
||
<span class="medgenPMjournal">Clin Neurol Neurosurg</span>
|
||
2013 Nov;115(11):2388-9.
|
||
Epub 2013 Aug 27
|
||
doi: 10.1016/j.clineuro.2013.08.017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24035686" target="_blank">24035686</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14550762">A proposed inhalation reference concentration for methanol.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Starr TB,
|
||
Festa JL</span><br />
|
||
<span class="medgenPMjournal">Regul Toxicol Pharmacol</span>
|
||
2003 Oct;38(2):224-31.
|
||
doi: 10.1016/s0273-2300(03)00095-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14550762" target="_blank">14550762</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20rib%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 (54)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29752917">Robotically Assisted Transthoracic Cervical Rib Resection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wybaillie E,
|
||
Maene L,
|
||
Cooreman F,
|
||
Beelen R</span><br />
|
||
<span class="medgenPMjournal">Ann Thorac Surg</span>
|
||
2018 Nov;106(5):e253-e255.
|
||
Epub 2018 May 9
|
||
doi: 10.1016/j.athoracsur.2018.04.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29752917" target="_blank">29752917</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28005137">Adverse Fetal and Neonatal Outcome and an Abnormal Vertebral Pattern: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schut PC,
|
||
Cohen-Overbeek TE,
|
||
Galis F,
|
||
Ten Broek CM,
|
||
Steegers EA,
|
||
Eggink AJ</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol Surv</span>
|
||
2016 Dec;71(12):741-750.
|
||
doi: 10.1097/OGX.0000000000000388.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28005137" target="_blank">28005137</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27975060">The Epidemiological, Morphological, and Clinical Aspects of the Cervical Ribs in Humans.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Spadliński Ł,
|
||
Cecot T,
|
||
Majos A,
|
||
Stefańczyk L,
|
||
Pietruszewska W,
|
||
Wysiadecki G,
|
||
Topol M,
|
||
Polguj M</span><br />
|
||
<span class="medgenPMjournal">Biomed Res Int</span>
|
||
2016;2016:8034613.
|
||
Epub 2016 Nov 15
|
||
doi: 10.1155/2016/8034613.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27975060" target="_blank">27975060</a><a href="/pmc/articles/PMC5126392" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23716186">Thoracic outlet syndrome: a neurological and vascular disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Klaassen Z,
|
||
Sorenson E,
|
||
Tubbs RS,
|
||
Arya R,
|
||
Meloy P,
|
||
Shah R,
|
||
Shirk S,
|
||
Loukas M</span><br />
|
||
<span class="medgenPMjournal">Clin Anat</span>
|
||
2014 Jul;27(5):724-32.
|
||
Epub 2013 May 29
|
||
doi: 10.1002/ca.22271.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23716186" target="_blank">23716186</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3394894">Thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sellke FW,
|
||
Kelly TR</span><br />
|
||
<span class="medgenPMjournal">Am J Surg</span>
|
||
1988 Jul;156(1):54-7.
|
||
doi: 10.1016/s0002-9610(88)80172-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3394894" target="_blank">3394894</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20rib%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 (59)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38704183">Thoracic outlet syndrome in women.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mulatti GC,
|
||
Dalio MB,
|
||
de Moraes TM,
|
||
Attie GA,
|
||
Brito-Queiroz A,
|
||
Joviliano EE</span><br />
|
||
<span class="medgenPMjournal">Semin Vasc Surg</span>
|
||
2024 Mar;37(1):44-49.
|
||
Epub 2024 Feb 2
|
||
doi: 10.1053/j.semvascsurg.2024.01.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38704183" target="_blank">38704183</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38704178">A review of arterial thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Potluri VK,
|
||
Li RD,
|
||
Crisostomo P,
|
||
Bechara CF</span><br />
|
||
<span class="medgenPMjournal">Semin Vasc Surg</span>
|
||
2024 Mar;37(1):12-19.
|
||
Epub 2024 Feb 13
|
||
doi: 10.1053/j.semvascsurg.2024.02.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38704178" target="_blank">38704178</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37109665">Anatomical Variants Identified on Computed Tomography of Oropharyngeal Carcinoma Patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Janta S,
|
||
Suwannakhan A,
|
||
Yurasakpong L,
|
||
Chaiyamoon A,
|
||
Kruepunga N,
|
||
Iwanaga J,
|
||
Tubbs RS,
|
||
Eiamratchanee P,
|
||
Paensukyen T</span><br />
|
||
<span class="medgenPMjournal">Medicina (Kaunas)</span>
|
||
2023 Apr 4;59(4)
|
||
doi: 10.3390/medicina59040707.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37109665" target="_blank">37109665</a><a href="/pmc/articles/PMC10144055" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36574580">Elective brachial plexus decompression in neurogenic thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Diner C,
|
||
Mathieu L,
|
||
Vandendries C,
|
||
Oberlin C,
|
||
Belkheyar Z</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2023 Feb;42(1):9-14.
|
||
Epub 2022 Nov 26
|
||
doi: 10.1016/j.hansur.2022.11.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36574580" target="_blank">36574580</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28005137">Adverse Fetal and Neonatal Outcome and an Abnormal Vertebral Pattern: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schut PC,
|
||
Cohen-Overbeek TE,
|
||
Galis F,
|
||
Ten Broek CM,
|
||
Steegers EA,
|
||
Eggink AJ</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol Surv</span>
|
||
2016 Dec;71(12):741-750.
|
||
doi: 10.1097/OGX.0000000000000388.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28005137" target="_blank">28005137</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20rib%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 (56)</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/38428008">Pediatric thoracic outlet syndrome: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Price A,
|
||
Fredricks N,
|
||
Truong N,
|
||
North RY</span><br />
|
||
<span class="medgenPMjournal">J Neurosurg Pediatr</span>
|
||
2024 May 1;33(5):484-495.
|
||
Epub 2024 Mar 1
|
||
doi: 10.3171/2024.2.PEDS23511.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38428008" target="_blank">38428008</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30122304">Outcomes of Surgical Management of Neurogenic Thoracic Outlet Syndrome: A Systematic Review and Bayesian Perspective.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yin ZG,
|
||
Gong KT,
|
||
Zhang JB</span><br />
|
||
<span class="medgenPMjournal">J Hand Surg Am</span>
|
||
2019 May;44(5):416.e1-416.e17.
|
||
Epub 2018 Aug 16
|
||
doi: 10.1016/j.jhsa.2018.06.120.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30122304" target="_blank">30122304</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28005137">Adverse Fetal and Neonatal Outcome and an Abnormal Vertebral Pattern: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schut PC,
|
||
Cohen-Overbeek TE,
|
||
Galis F,
|
||
Ten Broek CM,
|
||
Steegers EA,
|
||
Eggink AJ</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol Surv</span>
|
||
2016 Dec;71(12):741-750.
|
||
doi: 10.1097/OGX.0000000000000388.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28005137" target="_blank">28005137</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25427003">Treatment for thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Povlsen B,
|
||
Hansson T,
|
||
Povlsen SD</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2014 Nov 26;2014(11):CD007218.
|
||
doi: 10.1002/14651858.CD007218.pub3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25427003" target="_blank">25427003</a><a href="/pmc/articles/PMC11245746" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20091624">Treatment for thoracic outlet syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Povlsen B,
|
||
Belzberg A,
|
||
Hansson T,
|
||
Dorsi M</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2010 Jan 20;(1):CD007218.
|
||
doi: 10.1002/14651858.CD007218.pub2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20091624" target="_blank">20091624</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20rib%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 (5)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
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|
||
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/search?index=entry&start=1&limit=10&sort=score%20desc&field=number&search=117900" target="_blank">OMIM</a></li><li><a href="https://clinicaltrials.gov/search?cond=Cervical%20rib" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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|
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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=(%22cervical%20rib%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(%22Cervical%20rib%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></div>
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|
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<div class="portlet_content ln"><ul><li><a href="https://catalog.coriell.org/Search?q=117900" target="_blank">Coriell Institute for Medical Research</a></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://www.malacards.org/card/cervical_rib" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Cervical%20rib" target="_blank">MedlinePlus</a></li></ul></div>
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<a href="/pubmed/clinical?term=Cervical%20rib" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Cervical%20rib%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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<h3>Related information</h3>
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<a class="brieflinkpopperctrl" href="/mesh?LinkName=medgen_mesh&from_uid=102359" ref="log$=recordlinks">MeSH</a>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d373ef2f30673f7bb909dc">Cervical rib</a>
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<div class="tertiary">MedGen</div>
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