Microtia, Hearing Impairment, And Cleft Palate
Description
This syndrome is characterized by the association of bilateral microtia with severe to profound hearing impairment, and cleft palate.
Genes related to Microtia, Hearing Impairment, And Cleft Palate
- HOXA2
Clinical Features
Phenotypes and symptoms related to Microtia, Hearing Impairment, And Cleft Palate
- Hearing impairment
- Cleft palate
- Abnormality of the pinna
- Microtia
- Mixed hearing impairment
- Facial paralysis
- Profound hearing impairment
Incidence and onset information
— Not enough data available about incidence and published cases.
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Microtia, Hearing Impairment, And Cleft Palate Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
qGenEx Craniofacial Anomalies.
By Quantitative Genomic Medicine Laboratories, SL in Spain.
RECQL4, EYA1, COL2A1, PAX6, FOXC1, PITX2, OTX2, SHH, DHODH, BCOR, CTSK, FGFR3, CHD7, GJB6, IKBKG, PORCN, RUNX2, FGFR2, RAD21, SMC3 , (...)
View the complete list with 116 more genes
Specificity
1 %
Genes
100 % |
HOXA2.
By Fulgent Genetics Fulgent Genetics in United States.
HOXA2
Specificity
100 %
Genes
100 % |
Microtia , Sequencing HOXA2 Gene.
By Reference Laboratory Genetics in Spain.
HOXA2
Specificity
100 %
Genes
100 % |
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