1. Mendelian
  2. Rare Diseases
  3. FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD

Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction; Fpvepd

Table of contents:

Genes related to Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction; Fpvepd

  • TUBB6

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction; Fpvepd

  • Ptosis
  • Facial palsy
  • Bilateral ptosis
  • Hypomimic face
  • Velopharyngeal insufficiency
  • Nasal regurgitation
  • Bilateral facial palsy
  • Broad uvula

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction; Fpvepd Recommended genes panels

Panel Name, Specifity and genes Tested/covered
TUBB6.

By Fulgent Genetics Fulgent Genetics (United States).

TUBB6
Specificity
100 %
Genes
100 %

You can get up to -7 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

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