Isolated Scaphocephaly
Description
Isolated scaphocephaly is a form of nonsyndromic craniosynostosis characterized by premature fusion of the sagittal suture.
Clinical Features
Phenotypes and symptoms related to Isolated Scaphocephaly
- Frontal bossing
- Dolichocephaly
- Increased intracranial pressure
- Prominent occiput
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
Isolated Scaphocephaly Is also known as isolated dolichocephaly, non-syndromic sagittal synostosis.
Researches and researchers
Doctors, researchs, and experts related to Isolated Scaphocephaly extracted from public data.
Isolated Scaphocephaly Experts map
Current Researchs and researchers
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ROTTERDAM — Pr I.M.J. [Irene] MATHIJSSEN
Coordinator of expert centre - Investigator of research project - Coordinator of expert centre network
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Institution/s:
— Sophia Kinderziekenhuis, Erasmus MC - Erasmus Medisch Centrum -
Research area/topic::
Optimal treatment for sagittal suture synostosis (scaphocephaly)
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Institution/s:
Isolated Scaphocephaly Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Craniofacial Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
RUNX2, SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, ALX1, CD96, CDC45, WDR19, FAM20C, WDR35, IFT43, DPH1, EFNB1, MEGF8, ERF , (...)
View the complete list with 11 more genes
Specificity
10 %
Genes
100 % |
Craniofacial Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
RUNX2, SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, ALX1, CD96, CDC45, WDR19, FAM20C, WDR35, IFT43, DPH1, EFNB1, MEGF8, ERF , (...)
View the complete list with 11 more genes
Specificity
10 %
Genes
100 % |
Craniosynostosis.
By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center (United States).
RUNX2, SKI, TCF12, TGFBR1, TGFBR2, TWIST1, ZIC1, IFT122, RAB23, CDC45, ASXL1, WDR19, FREM1, WDR35, IFT43, EFNB1, MEGF8, ERF, FGFR1, FGFR2 , (...)
View the complete list with 7 more genes
Specificity
8 %
Genes
67 % |
Craniosynostosis Sequence Analysis.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
RUNX2, SKI, TCF12, TWIST1, ZIC1, IFT122, RAB23, CD96, SPECC1L, WDR35, IFT43, EFNB1, MEGF8, ERF, MSX2, POR, RECQL4
Specificity
12 %
Genes
67 % |
Craniofacial Del/Dup Panel.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
RUNX2, SALL1, SF3B4, SIX1, SIX5, SKI, SNRPB, TCF12, TCOF1, TWIST1, ZIC1, IFT122, RAB23, ALX1, CD96, POLR1A, WDR19, EVC2, POLR1C, POLR1D , (...)
View the complete list with 22 more genes
Specificity
8 %
Genes
100 % |
Craniosynostosis Del/Dup Panel.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
RUNX2, SKI, TCF12, TWIST1, ZIC1, IFT122, RAB23, CD96, SPECC1L, WDR35, IFT43, EFNB1, MEGF8, ERF, MSX2, POR, RECQL4
Specificity
12 %
Genes
67 % |
Craniosynostosis Seq + Del/Dup Panel.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
RUNX2, SKI, TCF12, TWIST1, ZIC1, IFT122, RAB23, CD96, SPECC1L, WDR35, IFT43, EFNB1, MEGF8, ERF, MSX2, POR, RECQL4
Specificity
12 %
Genes
67 % |
Craniofacial Seq + Del/Dup Panel.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
RUNX2, SALL1, SF3B4, SIX1, SIX5, SKI, SNRPB, TCF12, TCOF1, TWIST1, ZIC1, IFT122, RAB23, ALX1, CD96, POLR1A, WDR19, EVC2, POLR1C, POLR1D , (...)
View the complete list with 22 more genes
Specificity
8 %
Genes
100 % |
You can get up to 93 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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