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Primary Ciliary Dyskinesia.
Shoemark A, Harman K. Shoemark A, et al. Semin Respir Crit Care Med. 2021 Aug;42(4):537-548. doi: 10.1055/s-0041-1730919. Epub 2021 Jul 14. Semin Respir Crit Care Med. 2021. PMID: 34261178
Primary ciliary dyskinesia (PCD) is an inherited cause of bronchiectasis. ...It is likely that evidence-based PCD-specific management guidelines and therapies will be developed in the near future. This article examines prevalence, clinical features, di …
Primary ciliary dyskinesia (PCD) is an inherited cause of bronchiectasis. ...It is likely that evidence-based PCD-speci …
Diagnosis of primary ciliary dyskinesia: potential options for resource-limited countries.
Rumman N, Jackson C, Collins S, Goggin P, Coles J, Lucas JS. Rumman N, et al. Eur Respir Rev. 2017 Jan 17;26(143):160058. doi: 10.1183/16000617.0058-2016. Print 2017 Jan. Eur Respir Rev. 2017. PMID: 28096286 Free PMC article. Review.
Primary ciliary dyskinesia is a genetic disease of ciliary function leading to chronic upper and lower respiratory tract symptoms. The diagnosis is frequently overlooked because the symptoms are nonspecific and the knowledge about the disease in the …
Primary ciliary dyskinesia is a genetic disease of ciliary function leading to chronic upper and lower respirato …
Clinical care for primary ciliary dyskinesia: current challenges and future directions.
Rubbo B, Lucas JS. Rubbo B, et al. Eur Respir Rev. 2017 Sep 6;26(145):170023. doi: 10.1183/16000617.0023-2017. Print 2017 Sep 30. Eur Respir Rev. 2017. PMID: 28877972 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a rare genetic disease that affects the motility of cilia, leading to impaired mucociliary clearance. ...In this review, we provide a critical overview of the available literature on clinical care for PCD pati …
Primary ciliary dyskinesia (PCD) is a rare genetic disease that affects the motility of cilia, leading to impair …
Clinical features and management of children with primary ciliary dyskinesia in England.
Rubbo B, Best S, Hirst RA, Shoemark A, Goggin P, Carr SB, Chetcuti P, Hogg C, Kenia P, Lucas JS, Moya E, Narayanan M, O'Callaghan C, Williamson M, Walker WT; English National Children’s PCD Management Service. Rubbo B, et al. Arch Dis Child. 2020 Aug;105(8):724-729. doi: 10.1136/archdischild-2019-317687. Epub 2020 Mar 10. Arch Dis Child. 2020. PMID: 32156696
OBJECTIVE: In England, the National Health Service commissioned a National Management Service for children with primary ciliary dyskinesia (PCD). The aims of this study were to describe the health of children seen in this Service and compare lung function to …
OBJECTIVE: In England, the National Health Service commissioned a National Management Service for children with primary ciliary …
Fertility care among people with primary ciliary dyskinesia.
Schreck LD, Goutaki M, Jörger P, Dexter K, Manion M, Christin-Maitre S, Maitre B; COVID-PCD Patient Advisory Group; Kuehni CE, Pedersen ESL. Schreck LD, et al. Pediatr Pulmonol. 2024 Feb;59(2):281-290. doi: 10.1002/ppul.26743. Epub 2023 Nov 7. Pediatr Pulmonol. 2024. PMID: 37933800
INTRODUCTION: Fertility care is important for people living with primary ciliary dyskinesia (PCD) who are at increased risk of fertility problems. ...CONCLUSION: People with PCD are inconsistently referred to fertility specialists. We recommend care …
INTRODUCTION: Fertility care is important for people living with primary ciliary dyskinesia (PCD) who are at inc …
Clinical characteristics and genetic spectrum of 26 individuals of Chinese origin with primary ciliary dyskinesia.
Zhao X, Bian C, Liu K, Xu W, Liu Y, Tian X, Bai J, Xu KF, Zhang X. Zhao X, et al. Orphanet J Rare Dis. 2021 Jul 1;16(1):293. doi: 10.1186/s13023-021-01840-2. Orphanet J Rare Dis. 2021. PMID: 34210339 Free PMC article.
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare, highly heterogeneous genetic disorder involving the impairment of motile cilia. ...Biallelic pathogenic mutations were identified in 19 of the 26 patients, including 8 recorded HGMD mutations and …
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare, highly heterogeneous genetic disorder involving the impairment …
Comparison of the Lung Clearance Index in Preschool Children With Primary Ciliary Dyskinesia and Cystic Fibrosis.
Roehmel JF, Doerfler FJ, Koerner-Rettberg C, Brinkmann F, Schlegtendal A, Wetzke M, Rudolf I, Helms S, Große-Onnebrink J, Yu Y, Nuesslein T, Wojsyk-Banaszak I, Becker S, Eickmeier O, Sommerburg O, Omran H, Stahl M, Mall MA. Roehmel JF, et al. Chest. 2022 Sep;162(3):534-542. doi: 10.1016/j.chest.2022.02.052. Epub 2022 Mar 7. Chest. 2022. PMID: 35271842
BACKGROUND: Previous studies showed that the lung clearance index (LCI) determined by multiple-breath washout (MBW) is sensitive to detecting early lung disease in preschool children with cystic fibrosis (CF). In preschool children with primary ciliary dyskinesia …
BACKGROUND: Previous studies showed that the lung clearance index (LCI) determined by multiple-breath washout (MBW) is sensitive to detectin …
Primary ciliary dyskinesia: clinical criteria indicating ultrastructural studies.
Busquets RM, Caballero-Rabasco MA, Velasco M, Lloreta J, García-Algar Ó. Busquets RM, et al. Arch Bronconeumol. 2013 Mar;49(3):99-104. doi: 10.1016/j.arbres.2012.10.007. Epub 2012 Dec 23. Arch Bronconeumol. 2013. PMID: 23265970 English, Spanish.
INTRODUCTION: Primary ciliary dyskinesia (PCD) is a congenital disease characterized by impaired ciliary function, which involves a wide range of symptoms that are mainly respiratory. Recent articles that base diagnosis on ciliary ultrastructura …
INTRODUCTION: Primary ciliary dyskinesia (PCD) is a congenital disease characterized by impaired ciliary functio …
Presentation of primary ciliary dyskinesia in children: 30 years' experience.
Hosie PH, Fitzgerald DA, Jaffe A, Birman CS, Rutland J, Morgan LC. Hosie PH, et al. J Paediatr Child Health. 2015 Jul;51(7):722-6. doi: 10.1111/jpc.12791. Epub 2014 Dec 15. J Paediatr Child Health. 2015. PMID: 25510893
AIM: Primary ciliary dyskinesia (PCD) is a rare (1:15,000) condition resulting in recurrent suppurative respiratory tract infections, progressive lung damage and hearing impairment. ...Situs abnormalities and neonatal respiratory distress were present togethe …
AIM: Primary ciliary dyskinesia (PCD) is a rare (1:15,000) condition resulting in recurrent suppurative respiratory tra …
Accuracy of Nasal Nitric Oxide Measurement as a Diagnostic Test for Primary Ciliary Dyskinesia. A Systematic Review and Meta-analysis.
Shapiro AJ, Josephson M, Rosenfeld M, Yilmaz O, Davis SD, Polineni D, Guadagno E, Leigh MW, Lavergne V. Shapiro AJ, et al. Ann Am Thorac Soc. 2017 Jul;14(7):1184-1196. doi: 10.1513/AnnalsATS.201701-062SR. Ann Am Thorac Soc. 2017. PMID: 28481653 Free PMC article. Review.
RATIONALE: Primary ciliary dyskinesia (PCD) is a rare disorder causing chronic otosinopulmonary disease, generally diagnosed through evaluation of respiratory ciliary ultrastructure and/or genetic testing. ...OBJECTIVES: To perform a systematic review …
RATIONALE: Primary ciliary dyskinesia (PCD) is a rare disorder causing chronic otosinopulmonary disease, generally diag …
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