pierre robin syndrome | Pierre Robin Syndrome

Keyword	CPC	PCC	Volume	Score	Length of keyword
pierre robin syndrome	1.66	0.7	9678	99	21
pierre	1.39	0.3	8189	7	6
robin	1.9	0.2	6209	85	5
syndrome	1.34	0.4	4907	76	8

Keyword	CPC	PCC	Volume	Score
pierre robin syndrome	1.19	0.5	4092	62
pierre robin syndrome icd 10	0.26	0.4	3936	39
pierre robin syndrome life expectancy	1.34	0.6	112	51
pierre robin syndrome symptoms	1.28	0.4	4810	43
pierre robin syndrome treatment	0.71	0.1	6303	13
pierre robin syndrome triad	0.53	0.2	4757	52
pierre robin syndrome nhs	0.73	0.6	122	30
pierre robin syndrome pictures	1.59	0.1	4350	96
pierre robin syndrome genetics	1.53	0.3	6153	93
pierre robin syndrome cleft palate	1.17	0.1	5935	59
pierre robin syndrome seizure	1.95	0.1	3545	81
pierre robin syndrome adalah	0.64	0.3	8642	11
pierre robin syndrome developmental delays	1.49	0.8	5601	95
pierre robin syndrome learning difficulties	0.8	0.4	7731	67
pierre robin sequence syndrome	1.42	0.6	7437	34
what is pierre robin syndrome	1.32	0.5	3795	32
management of pierre robin syndrome	0.7	0.8	8064	2

Search Results related to pierre robin syndrome on Search Engine

Pierre Robin Syndrome - Cleveland Clinic
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/21863-pierre-robin-syndrome

WEBPierre Robin syndrome (PRS) — also called Pierre Robin sequence — is a condition in which your baby has a small jaw (micrognathia), a tongue that falls back toward the throat (glossoptosis) and upper airway obstruction.

DA: 86 PA: 4 MOZ Rank: 17

Pierre Robin Sequence | Johns Hopkins Medicine
hopkinsmedicine.org

https://www.hopkinsmedicine.org/health/conditions-and-diseases/pierre-robin-sequence

WEBPierre Robin sequence is also known as Pierre Robin syndrome or Pierre Robin malformation. It is a rare congenital birth defect characterized by an underdeveloped jaw, backward displacement of the tongue and upper airway obstruction. Cleft palate is also commonly present in children with Pierre Robin sequence.

DA: 17 PA: 26 MOZ Rank: 92

Pierre Robin Syndrome - StatPearls - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK562213/

WEBAug 7, 2023 · It is an autosomal dominant condition defined as a mutation of COL genes, affecting collagen formation. Clinical features include flat midface, epicanthal folds, retinal detachments, cataracts, joint hypermobility, and sensorineural hearing loss, in addition to the typical signs of PRS.

DA: 33 PA: 20 MOZ Rank: 35

Pierre Robin Syndrome | Children's Hospital of Philadelphia
chop.edu

https://www.chop.edu/conditions-diseases/pierre-robin-syndrome

WEBWhat is Pierre Robin syndrome? Pierre Robin syndrome is a congenital condition recently linked to genetic anomalies at chromosomes 2, 11 or 17. Often called Pierre Robin sequence, the disease is a chain of developmental malformations, each leading to the next.

DA: 3 PA: 40 MOZ Rank: 4

Pierre Robin Sequence | Causes, Symptoms, Diagnosis
cincinnatichildrens.org

https://www.cincinnatichildrens.org/health/p/pierre-robin-sequence

WEBWhat is Pierre Robin Sequence? Pierre Robin sequence is a set of abnormalities in a baby that develops during pregnancy. It is called a sequence because one of its features − an undeveloped lower jaw − starts off a sequence of other malformations while a baby is developing in utero.

DA: 11 PA: 21 MOZ Rank: 65

Pierre Robin sequence - Wikipedia
wikipedia.org

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

WEBPierre Robin sequence (/ p j ɛər r ɔː ˈ b æ̃ /; abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities. The three main features are micrognathia (abnormally small mandible ), which causes glossoptosis (downwardly displaced or retracted tongue), which in turn causes breathing problems due ...

DA: 91 PA: 60 MOZ Rank: 15

Pierre Robin Sequence - Symptoms, Causes, Treatment | NORD
rarediseases.org

https://rarediseases.org/rare-diseases/pierre-robin-sequence/

WEBAug 6, 2018 · Pierre Robin sequence (PRS) is characterized by a small lower jaw (micrognathia) and displacement of the tongue toward the back of the oral cavity (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate). PRS is believed to be caused by multiple contributing factors, which lead to a …

DA: 2 PA: 84 MOZ Rank: 98

Pierre-Robin Syndrome | Texas Children’s
texaschildrens.org

https://www.texaschildrens.org/content/conditions/pierre-robin-syndrome

WEBPierre-Robin Syndrome (PRS), also known as Pierre Robin sequence, is a congenital condition that affects the lower jaw and palate. The three main features that characterize PRS are: cleft palate (opening in the roof of the mouth) severe underdevelopment of the lower jaw (retrognathia)

DA: 17 PA: 20 MOZ Rank: 13

Pierre Robin Syndrome | St. Louis Children's Hospital
stlouischildrens.org

https://www.stlouischildrens.org/conditions-treatments/pierre-robin-syndrome

WEBWhat is Pierre Robin Syndrome? Pierre Robin in 1923 is credited as being the first to describe Robin sequence: a small jaw, leading to a tongue that falls back in the throat and upper airway obstruction. Cleft palate is not an obligatory finding, it occurs in up to 90% of patients with Robin sequence. Presumably, the palatal is intrinsically ...

DA: 33 PA: 23 MOZ Rank: 76

Pierre Robin sequence - UCSF Benioff Children's Hospital
ucsfbenioffchildrens.org

https://www.ucsfbenioffchildrens.org/conditions/pierre-robin-sequence

WEBOverview. Pierre Robin sequence, also known as Pierre Robin complex or syndrome, is a birth defect characterized by a wide, U-shaped cleft palate, a small lower jaw and a tongue that tends to fall back toward the throat, potentially obstructing the airway.

DA: 16 PA: 76 MOZ Rank: 43