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.

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.


Mendelian

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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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