Robinow-sorauf Syndrome

Clinical Features

Top most frequent phenotypes and symptoms related to Robinow-sorauf Syndrome

  • Hypertelorism
  • Strabismus
  • Malar flattening
  • Flat face
  • Plagiocephaly
  • Broad hallux
  • Long nose
  • Shallow orbits
  • Narrow nose
  • Craniofacial dysostosis

And another 1 symptoms. If you need more information about this disease we can help you.

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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.

Alternative names

Robinow-sorauf Syndrome Is also known as acrocephalosyndactyly, robinow-sorauf type, craniosynostosis-bifid hallux syndrome.

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.


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Robinow-sorauf Syndrome Recommended genes panels

Panel Name, Specifity and genes Tested/covered
NGS Craniosynostosis Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

TWIST1, RAB23, FGFR1, FGFR2, MSX2, POR, RECQL4
Specificity
15 %
Genes
100 %
Saethre-Chotzen syndrome.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

TWIST1
Specificity
100 %
Genes
100 %
Saethre-Chotzen Syndrome - TWIST1 Sequencing.

By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado (United States).

TWIST1
Specificity
100 %
Genes
100 %
Test for Saethre-Chotzen Syndrome.

By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands).

TWIST1
Specificity
100 %
Genes
100 %
Saethre-Chotzen Syndrome.

By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital (United States).

TWIST1, FGFR2, FGFR3
Specificity
34 %
Genes
100 %
Saethre-Chotzen Syndrome - Twist Gene Analysis.

By Center for Genetics at Saint Francis Saint Francis Hospital (United States).

TWIST1
Specificity
100 %
Genes
100 %
Craniodysmorphology Panel (FGFR1,2,3,TWIST).

By Center for Genetics at Saint Francis Saint Francis Hospital (United States).

TWIST1, FGFR2
Specificity
50 %
Genes
100 %
Craniosynostosis.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).

SKI, TGFBR1, TGFBR2, TWIST1, IFT122, RAB23, ASXL1, WDR19, WDR35, IFT43, EFNB1, FBN1, FGFR1, FGFR2, FGFR3, GLI3, ALPL, ALX4, IL11RA, MASP1 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM ORPHANET MESH Genetic Syndrome Finder

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