Ehlers-danlos Syndrome With Periventricular Heterotopia
Description
Ehlers-Danlos syndrome (EDS) with periventricular heterotopia is a newly described variant of EDS.
Genes related to Ehlers-danlos Syndrome With Periventricular Heterotopia
- FLNA
Clinical Features
Top most frequent phenotypes and symptoms related to Ehlers-danlos Syndrome With Periventricular Heterotopia
- Scoliosis
- Hernia
- Patent ductus arteriosus
- Gastroesophageal reflux
- Joint hypermobility
- Abnormal bleeding
- Focal-onset seizure
- Thin skin
- Aortic regurgitation
- Pyloric stenosis
And another 6 symptoms. If you need more information about this disease we can help you.
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
Ehlers-danlos Syndrome With Periventricular Heterotopia Is also known as eds with periventricular heterotopia.
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.Ehlers-danlos Syndrome With Periventricular Heterotopia Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Epilepsy Advanced Sequencing and CNV Evaluation - Developmental Brain Malformations.
By Athena Diagnostics Inc (United States).
SHH, STIL, SIX3, TUBA8, SLC25A19, DEAF1, ARFGEF2, RAB3GAP1, CENPJ, NDE1, FKRP, ARX, ASPM, POMGNT1, POMT2, TUBA1A, COL4A1, CPT2, WDR62, DCX , (...)
View the complete list with 20 more genes
Specificity
3 %
Genes
100 % |
Epilepsy Advanced Sequencing and CNV Evaluation.
By Athena Diagnostics Inc (United States).
SCN1A, SCN1B, SCN2A, SCN3A, SCN5A, SCN8A, SCN9A, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SLC2A1, SLC35A2, SLC6A1, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS , (...)
View the complete list with 214 more genes
Specificity
1 %
Genes
100 % |
NGS XLID Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TAF1, TIMM8A, TSPAN7, MED12, UBE2A, USP9X, ZMYM3, ZNF41, ZNF711 , (...)
View the complete list with 94 more genes
Specificity
1 %
Genes
100 % |
NGS Skeletal Dysplasia Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
SLC26A2, SOX9, TRPV4, COL1A2, COMP, FGFR3, FLNA, HSPG2
Specificity
13 %
Genes
100 % |
NGS Epilepsy/Seizure Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
SCN1A, SCN1B, SCN2A, SCN5A, SCN8A, SCN9A, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SLC2A1, SLC35A2, SLC9A6, SNAP25, SPTAN1, CDKL5, STXBP1, SYN1, SYNGAP1 , (...)
View the complete list with 124 more genes
Specificity
1 %
Genes
100 % |
FLNA-related disorders.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
FLNA
Specificity
100 %
Genes
100 % |
Periventricular Heterotopia, Ehlers-Danlos variant (FLNA).
By Center for Human Genetics, Inc (United States).
FLNA
Specificity
100 %
Genes
100 % |
Connective Tissue Disorders 22-gene panel.
By Center for Human Genetics, Inc (United States).
TGFB2, TGFBR1, TGFBR2, TGFBR3, ACTA2, NTM, COL11A1, COL11A2, COL1A2, COL3A1, COL5A1, COL5A2, FBN1, FBN2, FLNA, SMAD3, MYH11, MYLK, NOTCH1, PRKG1
Specificity
5 %
Genes
100 % |
You can get up to 211 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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