About: Williams–Campbell syndrome

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Williams–Campbell syndrome (WCS) is a disease of the airways where cartilage in the bronchi is defective. It is a form of congenital cystic bronchiectasis. This leads to collapse of the airways and bronchiectasis. It acts as one of the differential to allergic bronchopulmonary aspergillosis. WCS is a deficiency of the bronchial cartilage distally.

Attributes	Values
rdf:type	Thing Fuchs' dystrophy yago:WikicatBronchusDisorders yago:Abstraction100002137 yago:Attribute100024264 yago:Condition113920835 yago:Disorder114052403 yago:PhysicalCondition114034177 disease yago:State100024720
rdfs:label	متلازمة ويليامز كامبل (ar) Williams-Campbell-Syndrom (de) Sindrome di Williams-Campbell (it) Williams–Campbell syndrome (en)
rdfs:comment	متلازمة ويليامز كامبل (بالإنجليزية: Williams–Campbell syndrome)‏ هي مرض يصيب السبيل التنفسي بسبب ضرر يصيب غضاريف الشعب الهوائية. هذا يؤدي إلى انهيار السبيل التنفسي وتوسع القصبات. متلازمة ويليامز كامبل عبارة عن فضيع في الغضاريف القصبية. (ar) Das Williams-Campbell-Syndrom (WCS) ist eine sehr seltene angeborene Fehlbildung der Lunge, die durch eine generalisierte Aplasie, Hypoplasie oder Dysplasie der Knorpelspangen der Segment- und Subsegmentbronchien gekennzeichnet ist. Das Syndrom kann als Variante der Bronchomalazie angesehen werden. Die Namensbezeichnung (Eponym) bezieht sich auf die Autoren der Erstbeschreibung aus dem Jahre 1960, die australischen Pädiater Howard Williams und Peter Campbell. (de) Williams–Campbell syndrome (WCS) is a disease of the airways where cartilage in the bronchi is defective. It is a form of congenital cystic bronchiectasis. This leads to collapse of the airways and bronchiectasis. It acts as one of the differential to allergic bronchopulmonary aspergillosis. WCS is a deficiency of the bronchial cartilage distally. (en) La sindrome di Williams-Campbell (WCS) è una malattia delle vie aeree in cui la cartilagine nei bronchi è difettosa. È una forma di bronchiectasia cistica congenita. Ciò porta al collasso delle vie aeree e a bronchiectasie. Assomiglia all'aspergillosi broncopolmonare allergica. La WCS è una carenza della cartilagine bronchiale distale. (it)
foaf:name	Williams–Campbell syndrome (en)
name	Williams–Campbell syndrome (en)
dcterms:subject	Bronchus disorders Syndromes
Wikipage page ID	16109288 (xsd:integer)
Wikipage revision ID	1101724606 (xsd:integer)
Link from a Wikipage to another Wikipage	dbr:Carbon_dioxide Non-invasive Beta2-adrenergic agonist Corticosteroid Cough Chronic obstructive pulmonary disease Chronic respiratory failure Genetic mutation Anticholinergic Lung transplantation Clinical history Pathology Bronchial Bronchiectasis Bronchoscopy Bronchus disorders Lobectomy Airway Allergic bronchopulmonary aspergillosis Dyspnea Bronchomalacia Bronchus Diagnosis of exclusion Fuchs' dystrophy Family history Respiratory failure Lobar pneumonia Hypercapnia Hyperinflation Syndromes Physical therapy Cystic lung disease Operation of computed tomography Autosomal Recessive Cartilage Mainstem bronchus Toxic shock syndrome Lobes of the lung Non invasive positive pressure ventilation Congenital Lung disease Exacerbation Lung function Wheeze Bronchial tree Hospitalization Hyperosmolarity Leukotriene receptor antagonists Confirmatory test Home oxygen therapy Mucolytics
sameAs	Williams–Campbell syndrome Williams–Campbell syndrome Williams–Campbell syndrome Williams–Campbell syndrome Williams–Campbell syndrome Williams–Campbell syndrome
dbp:wikiPageUsesTemplate	dbt:Cn dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist
diagnosis	Bronchoscopy Diagnosis of exclusion
OMIM	211450 (xsd:integer)
onset	Typically childhood (en)
treatment	Lung transplantation
causes	Genetic mutation
frequency	Unknown but extremely rare (en)
synonyms	Bronchomalacia
has abstract	متلازمة ويليامز كامبل (بالإنجليزية: Williams–Campbell syndrome)‏ هي مرض يصيب السبيل التنفسي بسبب ضرر يصيب غضاريف الشعب الهوائية. هذا يؤدي إلى انهيار السبيل التنفسي وتوسع القصبات. متلازمة ويليامز كامبل عبارة عن فضيع في الغضاريف القصبية. (ar) Das Williams-Campbell-Syndrom (WCS) ist eine sehr seltene angeborene Fehlbildung der Lunge, die durch eine generalisierte Aplasie, Hypoplasie oder Dysplasie der Knorpelspangen der Segment- und Subsegmentbronchien gekennzeichnet ist. Das Syndrom kann als Variante der Bronchomalazie angesehen werden. Die Namensbezeichnung (Eponym) bezieht sich auf die Autoren der Erstbeschreibung aus dem Jahre 1960, die australischen Pädiater Howard Williams und Peter Campbell. (de) Williams–Campbell syndrome (WCS) is a disease of the airways where cartilage in the bronchi is defective. It is a form of congenital cystic bronchiectasis. This leads to collapse of the airways and bronchiectasis. It acts as one of the differential to allergic bronchopulmonary aspergillosis. WCS is a deficiency of the bronchial cartilage distally. (en) La sindrome di Williams-Campbell (WCS) è una malattia delle vie aeree in cui la cartilagine nei bronchi è difettosa. È una forma di bronchiectasia cistica congenita. Ciò porta al collasso delle vie aeree e a bronchiectasie. Assomiglia all'aspergillosi broncopolmonare allergica. La WCS è una carenza della cartilagine bronchiale distale. (it)
prevention	None (en)
risks	Family history
medical cause	Genetic mutation

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