bardet biedl syndrome | Bardet-Biedl syndrome - About the Disease

Keyword	CPC	PCC	Volume	Score	Length of keyword
bardet biedl syndrome	0.65	0.9	5115	34	21
bardet	0.19	0.8	5172	94	6
biedl	0.07	0.2	4268	13	5
syndrome	1.43	0.9	98	88	8

Keyword	CPC	PCC	Volume	Score
bardet biedl syndrome	1.11	0.5	6379	94
bardet biedl syndrome genereviews	1.55	0.8	3985	29
bardet-biedl syndrome symptoms	1.83	0.4	9070	83
bardet biedl syndrome life expectancy	0.22	0.2	2561	81
bardet biedl syndrome uk	1.29	1	1883	49
bardet biedl syndrome icd 10	1.57	0.4	3785	1
bardet biedl syndrome diagnosis	0.51	0.1	7800	82
bardet biedl syndrome radiology	1.93	0.3	8991	28
bardet biedl syndrome eye	1.66	0.8	4563	74
bardet biedl syndrome obesity	0.87	0.9	2734	75
bardet-biedl syndrome treatment	0.1	0.3	4548	37
bardet biedl syndrome omim	1.31	0.6	8334	2
bardet biedl syndrome mayo clinic	0.68	0.5	6481	77
bardet biedl syndrome genetics	0.99	1	8832	13
bardet biedl syndrome pronunciation	0.04	0.1	6331	47
laurence moon bardet biedl syndrome	1.71	0.6	1460	39
what is bardet biedl syndrome	1.96	0.3	5358	50

Search Results related to bardet biedl syndrome on Search Engine

Bardet-Biedl syndrome - About the Disease - Genetic and Rare …
nih.gov

https://rarediseases.info.nih.gov/diseases/6866/bardet-biedl-syndrome/

WEBSummary. Bardet-Biedl syndrome (BBS) is an inherited condition that affects many parts of the body. People with this syndrome have progressive visual impairment due to cone-rod dystrophy; extra fingers or toes (polydactyly); truncal obesity; decreased function of the male gonads (hypogonadism); kidney abnormalities; and learning difficulties.

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Bardet–Biedl syndrome - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Bardet%E2%80%93Biedl_syndrome

WEBBardet–Biedl syndrome (BBS) is a ciliopathic human genetic disorder that produces many effects and affects many body systems. It is characterized by rod/cone dystrophy, polydactyly, central obesity, hypogonadism, and kidney dysfunction in some cases.

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Bardet-Biedl syndrome: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome/

WEBBardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among members of the same family. Vision loss is one of the major features of Bardet-Biedl syndrome. Loss of vision occurs as the light-sensing tissue at the back of the eye ( the retina ...

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What is BBS? — Bardet Biedl Syndrome Foundation
bardetbiedl.org

https://www.bardetbiedl.org/what-is-bbs

WEBWhat is bardet biedl syndrome (BBS)? Bardet Biedl Syndrome is a rare genetic disorder with highly variable symptoms which may include retinal degeneration, obesity, reduced kidney function, polydactyly (extra digits of the hands or feet) among many other features.

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Bardet-Biedl Syndrome - Symptoms, Causes, Treatment | NORD
rarediseases.org

https://rarediseases.org/rare-diseases/bardet-biedl-syndrome/

WEBJul 12, 2022 · Summary. Bardet-Biedl syndrome (BBS) is a genetic condition that impacts multiple body systems. It is classically defined by six features. Patients with BBS can experience problems with obesity, specifically with fat deposition along the abdomen. They often also suffer from intellectual impairments.

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Bardet-Biedl Syndrome (BBS) - American Academy of Ophthalmology
aao.org

https://www.aao.org/education/disease-review/bardet-biedl-syndrome-bbs

WEBAug 26, 2016 · Clinical Findings. BBS is a ciliopathy with protean manifestations. Cilia gene mutations can cause a range of clinical conditions with retinal and renal dysfunction as common recurrent features.

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Bardet-Biedl Syndrome: Current Perspectives and Clinical Outlook
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896974/

WEBJan 30, 2023 · The Bardet Biedl syndrome (BBS) is a rare inherited disorder considered a model of non-motile ciliopathy. It is in fact caused by mutations of genes encoding for proteins mainly localized to the base of the cilium. Clinical features of BBS patients are widely shared with patients suffering from other ciliopathies, especially autosomal …

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Bardet-Biedl Syndrome Overview - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1363/

WEBJul 14, 2003 · Bardet-Biedl syndrome (BBS) is a multisystem non-motile ciliopathy primarily characterized by retinal cone-rod dystrophy, obesity and related complications, postaxial polydactyly, cognitive impairment, hypogonadotropic hypogonadism and/or genitourinary malformations, and renal malformations and/or renal parenchymal disease.

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Orphanet: Bardet-Biedl syndrome
orpha.net

https://www.orpha.net/en/disease/detail/110

WEBBardet-Biedl syndrome. Suggest an update. Disease definition. A rare genetic multisystem disorder characterized by the variable association of retinal dystrophy, obesity, polydactyly, genitourinary and kidney anomalies, learning disability and hypogonadism, with a wide spectrum of other minor manifestations. ORPHA:110.

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Bardet-Biedl syndrome - MedlinePlus
medlineplus.gov

https://medlineplus.gov/download/genetics/condition/bardet-biedl-syndrome.pdf

WEBDescription. Bardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among members of the same family. Vision loss is one of the …

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