kartagener syndrome | Kartagener Syndrome: Causes, Symptoms, and Treat

Keyword	CPC	PCC	Volume	Score	Length of keyword
kartagener syndrome	1.95	0.4	8277	76	19
kartagener	1.18	0.1	7368	29	10
syndrome	1.91	0.9	7831	71	8

Keyword	CPC	PCC	Volume	Score
kartagener syndrome	0.91	0.6	7639	73
kartagener syndrome triad	0.88	0.7	2082	47
kartagener syndrome radiology	0.26	0.8	51	83
kartagener syndrome symptoms	1.88	0.2	4523	26
kartagener syndrome infertility	0.3	0.8	2058	32
kartagener syndrome case report	0.32	0.4	2548	79
kartagener syndrome treatment	1.42	0.8	1515	33
kartagener syndrome radiopaedia	1.19	0.8	6961	27
kartagener syndrome icd 10	0.2	0.4	2085	30
kartagener syndrome pcd	0.2	0.3	4331	91
kartagener syndrome vs cystic fibrosis	1.19	0.1	9586	53
kartagener syndrome pronunciation	0.29	0.6	8645	2
kartagener syndrome inheritance	0.44	0.6	3276	100
kartagener syndrome life expectancy	0.31	0.3	9904	1
what is kartagener syndrome	1.75	0.5	4314	65
situs inversus in kartagener syndrome	1.77	0.9	5966	46
syndrome de kartagener	0.79	0.8	7534	8
kartagener syndrome dextrocardia	1.69	0.6	2995	80

Search Results related to kartagener syndrome on Search Engine

Kartagener Syndrome: Causes, Symptoms, and Treatment - WebMD
webmd.com

https://www.webmd.com/children/what-is-kartagener-syndrome

WEBFeb 20, 2024 · Kartagener syndrome is a type of primary ciliary dyskinesia or PCD, that may also cause reversed internal organs. This means your organs are on the opposite side of your body from where they...

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Kartagener syndrome: A case report - PMC - National Center for
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059757/

WEBApr 21, 2021 · Kartagener syndrome (KS) is a subset of a larger group of ciliary motility disorders called primary ciliary dyskinesias (PCDs) . KS is an inherited autosomal recessive disorder that causes defects in the action of ciliary movement, comprises of triad sinusitis, situs inversus, and bronchiectasis .

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GARD Rare Disease Information - Kartagener syndrome
rarediseases.org

https://rarediseases.org/gard-rare-disease/kartagener-syndrome/

WEBDisease Overview. Kartagener syndrome is a type of p rimary ciliary dyskinesia that is also characterized by situs inversus totalis (mirror-image reversal of internal organs).

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Kartagener's syndrome: A case series - PMC - National Center for
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519024/

WEBKartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder comprising the triad of situs inversus, chronic sinusitis, and bronchiectasis. The basic problem lies in the defective movement of cilia, leading to recurrent chest infections, ear/nose/throat symptoms, and infertility.

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Kartagener Syndrome Symptoms and Treatment - Verywell Health
verywellhealth.com

https://www.verywellhealth.com/kartagener-syndrome-2860366

WEBJul 10, 2022 · Kartagener syndrome is a very rare hereditary disorder that is caused by defects in the genes. It is autosomal recessive, meaning that it only occurs if both parents carry the gene. Kartagener syndrome affects approximately 30,000 people, including all …

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Primary ciliary dyskinesia - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Primary_ciliary_dyskinesia

WEBImmotile ciliary syndrome or Kartagener syndrome: Normal cilia (A) and cilia representative of Kartagener's syndrome (B) Specialty: Pulmonology Symptoms: Respiratory problems, chronic mucus-producing cough and runny nose. Complications: Chronic recurrent respiratory infections, including sinusitis, bronchitis, pneumonia, and …

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Kartagener syndrome - PMC - National Center for Biotechnology …
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056330/

WEBJan 12, 2011 · Kartagener syndrome is a rare, ciliopathic, autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the respiratory tract and fallopian tube. Patients usually present with chronic recurrent rhinosinusitis, otitis media, pneumonia, and bronchiectasis caused by pseudomonal infection.

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Kartagener Syndrome | St. Louis Children's Hospital
stlouischildrens.org

https://www.stlouischildrens.org/conditions-treatments/kartagener-syndrome

WEBKartagener syndrome, a rare inherited birth defect, is a type of primary ciliary dyskinesia (PCD), a condition marked by frequent infections of the lungs, ears, throat, and sinuses that continue into adulthood. About 50 percent of patients with PCD may have Kartagener's Syndrome.

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Primary Ciliary Dyskinesia | Children's Hospital of Philadelphia
chop.edu

https://www.chop.edu/conditions-diseases/primary-ciliary-dyskinesia

WEBWhen defects in the cilia are accompanied by the triad of situs inversus, chronic sinusitis, and bronchiectasis (dilation of the small airways) , the condition is known as Kartagener’s syndrome. Signs and symptoms of PCD. PCD is characterized by recurrent respiratory infections such as bronchitis and/or pneumonias.

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Primary Ciliary Dyskinesia (Kartagener Syndrome) - Medscape
medscape.com

https://emedicine.medscape.com/article/299299-overview

WEBJun 11, 2020 · Kartagener syndrome (KS) is inherited via an autosomal recessive pattern. Symptoms result from defective cilia motility. Also see Primary Ciliary Dyskinesia (pediatrics). Next: Pathophysiology....

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