Williams-Campbell syndrome




Input patient's signs and symptoms


Narrow down the case reports



Total: 20 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
4
(4.0%)
10410549
[Severe adult-type Williams-Campbell syndrome (Williams-Campbell-type bronchiectasis)].
Kimoto T, Kawamura T, Nakahara Y, Mochizuki Y.
Nihon Kokyuki Gakkai Zasshi. 1999;37(5):429-32.
Dyspnea
Bronchiectasis Fluoroscopy Homo sapiens Male Radiography, Thoracic Respiratory Insufficiency Syndrome X-Ray Computed Tomography
4
(4.0%)
9498979
Lung transplantation for Williams-Campbell syndrome.
Palmer SM Jr, Layish DT, Kussin PS, Oury T, Davis RD, Tapson VF.
Chest. 1998;113(2):534-7.
Pneumonia
Adult Airway Obstruction Bronchi Bronchial Diseases Bronchiectasis Cartilage Diseases Fatal Outcome Homo sapiens Ischemia Lung Transplantation Male Pneumonia, Bacterial Postoperative Complications Pseudomonas Infections Pseudomonas aeruginosa Pulmonary Emphysema Respiratory Insufficiency Syndrome
4
(4.0%)
9493457
[An adult case of Williams-Campbell syndrome associated with pulmonary hypertension and a severe decrease in ventilatory response].
Amano S, Yoshida Y, Shimizu H, Takeda T, Urabe N, Mizoo A, Kimura H, Kuriyama T.
Nihon Kyobu Shikkan Gakkai Zasshi. 1997;35(11):1265-70.
Hypertension
Adult Bronchial Diseases Bronchiectasis Cartilage Diseases Homo sapiens Hypercapnia Hypoxia Male Pulmonary Hypertension Respiratory Insufficiency Syndrome
4
(4.0%)
8797568
Mortality following adenotonsillectomy in a patient with Williams-Campbell syndrome.
Kirse DJ, Tryka AF, Seibert RW, Bower CM.
Arch Otolaryngol Head Neck Surg. 1996;122(9):1007-10.
Enlarged tonsils
Adenoidectomy Ambulatory Surgical Procedures Bronchiectasis Child Fatal Outcome Homo sapiens Hypertrophy Male Palatine Tonsil Syndrome Tonsillectomy
4
(4.0%)
8265276
Familial congenital bronchiectasis: Williams-Campbell syndrome.
Jones VF, Eid NS, Franco SM, Badgett JT, Buchino JJ.
Pediatr Pulmonol. 1993;16(4):263-7.
Bronchiectasis
Bronchi Bronchiectasis Child, Preschool Females Homo sapiens Infant, Newborn Syndrome
4
(4.0%)
6296528
[Irreversible generalized pulmonary emphysema resulting from destructive bronchitis and bronchiolitis following adenovirus infection].
Manzke H.
Klin Padiatr. 1982;194(6):387-92.
Emphysema
Adenovirus Infections Adenovirus Infections, Human Asthma Bronchiectasis Bronchiolitis, Viral Bronchitis Differential Diagnosis Homo sapiens Infant Male Pulmonary Emphysema Syndrome
4
(4.0%)
3597897
Congenital bronchiectasis due to cartilage deficiency: CT demonstration.
Watanabe Y, Nishiyama Y, Kanayama H, Enomoto K, Kato K, Takeichi M.
J Comput Assist Tomogr. 1987;11(4):701-3.
Bronchiectasis
Bronchi Bronchiectasis Females Homo sapiens Middle Aged Syndrome X-Ray Computed Tomography
4
(4.0%)
2232375
[Williams-Campbell syndrome complicated by multiple meniscus signs in an adult case; is it a characteristic finding?].
Fujishita M, Kataoka R, Kobayashi M, Miyoshi I.
Nihon Kyobu Shikkan Gakkai Zasshi. 1990;28(7):1018-23.
Pneumonia
Bronchi Bronchiectasis Females Homo sapiens Middle Aged Syndrome
4
(4.0%)
1856896
Case report: computed tomography findings in Williams-Campbell syndrome.
Kaneko K, Kudo S, Tashiro M, Kishikawa T, Nakanishi Y, Yamada H.
J Thorac Imaging. 1991;6(2):11-3.
Bronchiectasis
Bronchiectasis Cyst Homo sapiens Male Middle Aged Pulmonary Emphysema Syndrome X-Ray Computed Tomography
4
(4.0%)
937831
Probable familial congenital bronchiectasis due to cartilage deficiency (Williams-Campbell syndrome).
Wayne KS, Taussig LM.
Am Rev Respir Dis. 1976;114(1):15-22.
Bronchiectasis
Bronchi Bronchiectasis Bronchoscopy Females Homo sapiens Lung Male Respiratory Function Tests
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 8

HPO ID Term # of case reports
HP:0002110 Bronchiectasis 15
HP:0002878 Respiratory failure 4
HP:0002094 Dyspnea 2
HP:0002780 Bronchomalacia 2
HP:0000822 Hypertension 1
HP:0002097 Emphysema 1
HP:0002205 Recurrent respiratory infections 1
HP:0031245 Productive cough 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID