• Bifid Uvula

    Who are the top experts researching treatments for bifid uvula?

    The top experts researching bifid uvula are: Richard H. Schwartz, Robert J. Shprintzen and Lynn Hoch.

  • What are the top concepts researched in studies about bifid uvula?

    The most researched concepts in studies of bifid uvula are: Cleft Palate, Loeys-Dietz Syndrome, Arterial Tortuosity, Transforming Growth Factor and Developmental Delay.

  • What are some of the top places that specialize in bifid uvula?

    Recommended institutions that specialize in bifid uvula:

    1. ENT Specialists, P.C720 N 129th St, Omaha, NE 68154, United States Phone: +14024033094
    2. ENT Specialists6249 Grand River Ave, Brighton, MI 48114, United States Phone: +18108441900
    3. London ENT Clinic51 Harley St, London W1G 8QQ, United Kingdom Phone: +442072620297
    4. Otorrino. Dr. Juan Garcia-Valdecasas Bernal.Clínica SENT, Cam. de Rda., 39, 18004 Granada, Spain Phone: +34958264721

Recent articles about Bifid Uvula

Incidence Of Bifid Uvula And Its Relationship To Submucous Cleft Palate And A...

[ PUBLICATION ] ... Bifid uvula is a frequently observed anomaly in the general population and can be regarded as a marker for submucous cleft palate. OBJECTIVE: In this study aimed to determine the frequency ...
Known for
Bifid Uvula | Submucous Cleft Palate | Oral Cleft | 1206 Children

Morphologic Significance Of Bifid Uvula.

[ PUBLICATION ]
Known for
Bifid Uvula | Morphologic Significance | Submucous Cleft Palate | Marker Relationship

Prevalence Of Bifid Uvula In Primary School Children

[ PUBLICATION ] ... A bifid uvula is an anatomic variation that can be predictive of sub-mucous cleft palate, which may cause velopharyngeal insufficiency (VPI). Bifid uvula prevalence in the literature ...
Known for
Bifid Uvula | Primary Children | Sex Ratio | Velopharyngeal Insufficiency

The Bifid Uvula: Is It A Marker For An Otitis Prone Child?

[ PUBLICATION ] ... Isolated bifid uvula, without overt cleft palate, was detected among 44 children who had been followed in the practice during the first three years of life. A chart review was performed to ...
Known for
Bifid Uvula | Otitis Prone Child | Tympanostomy Tubes | Higher Proportion

De Novo Loss-Of-Function Mutations In Usp9x Cause A Female-Specific Recognizable...

[ PUBLICATION ] Mutations in more than a hundred genes have been reported to cause X-linked recessive intellectual disability (ID) mainly in males. In contrast, the number of identified X-linked genes in which ...
Known for
Function Mutations | Novo Loss | Female-Specific Recognizable Syndrome | Developmental Delay

Bifid Uvula: Prevalence And Association In Otitis Media With Effustion Inchildren...

[ PUBLICATION ] ... a bifid uvula as seen whilst under a general anaesthetic. The prevalence was found to be 7.5 per cent (53:709) which is higher than other published figures for a Caucasian population. ...
Known for
Bifid Uvula | Otitis Media | Effustion Inchildren | Otolaryngological Operations

Bifid Uvula And Familial Stickler Syndrome Diagnosed Prenatally Before The...

[ PUBLICATION ] ... the uvula may be technically difficult due to its anatomy and presence of surrounding structures. A cleft involving the soft palate and the uvula is one of the clinical features of ...
Known for
Stickler Syndrome | Bifid Uvula | Sign” Landmark | Soft Palate

Multiple Phenotypes In Phosphoglucomutase 1 Deficiency

[ PUBLICATION ] BACKGROUND: Congenital disorders of glycosylation are genetic syndromes that result in impaired glycoprotein production. We evaluated patients who had a novel recessive disorder of ...
Known for
1 Deficiency | Screening Test | Dietary Supplementation | Congenital Disorder

Bifid Uvula And Aortic Aneurysm

[ PUBLICATION ]
Known for
Bifid Uvula | Aortic Aneurysm

Aneurysm Syndromes Caused By Mutations In The Tgf-Β Receptor

[ PUBLICATION ] BACKGROUND: The Loeys-Dietz syndrome is a recently described autosomal dominant aortic-aneurysm syndrome with widespread systemic involvement. The disease is characterized by the triad of ...
Known for
Loeys-Dietz Syndrome | Tgf-Β Receptor | Vascular Ehlers | Natural History

 

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