1. Mendelian
  2. Rare Diseases
  3. CAPILLARY MALFORMATIONS, CONGENITAL; CMC

Capillary Malformations, Congenital; Cmc

Table of contents:

Description

Capillary malformations are a form of vascular malformation that are present from birth, tend to grow with the individual, do not regress spontaneously, and show normal rates of endothelial cell turnover. Capillary malformations are distinct from capillary hemangiomas (OMIM ), which are highly proliferative lesions that appear shortly after birth and show rapid growth, slow involution, and endothelial hypercellularity (Spring and Bentz, 2005; Legiehn and Heran, 2006).

Genes related to Capillary Malformations, Congenital; Cmc

  • GNAQ

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Capillary Malformations, Congenital; Cmc

  • Intellectual disability
  • Seizures
  • Scoliosis
  • Edema
  • Dilatation
  • Arrhythmia
  • Glaucoma
  • Papule
  • Nevus
  • Overgrowth

And another 19 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

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

Capillary Malformations, Congenital; Cmc Is also known as port-wine stain, nevi flammei, familial multiple, capillary malformations, cmal.

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.

Capillary Malformations, Congenital; Cmc Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Platelet Disorders.

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

RUNX1, STIM1, TBXA2R, TBXAS1, USF1, VPS33B, VWF, WAS, GP6, HPS3, HPS4, CD36, HPS5, DTNBP1, P2RY12, HPS6, MASTL, LYST, VIPAS39, FERMT3 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
100 %
Uveal Melanoma-Related NGS Gene Panel: GNAQ, GNA11 and BAP1.

By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine (United States).

GNA11, GNAQ, BAP1
Specificity
34 %
Genes
100 %
Somatic Overgrowth Gene Panel.

By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine (United States).

AKT1, AKT2, AKT3, MTOR, GNA11, GNAQ, PIK3CA, PIK3R2
Specificity
13 %
Genes
100 %
GNAQ.

By Institute for Human Genetics University Clinic Freiburg (Germany).

GNAQ
Specificity
100 %
Genes
100 %
Vascular Malformations NGS Multi-Gene Panel (21 Genes).

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands).

BMPR2, SOX18, TEK, GLMN, CAV1, KRIT1, ACVRL1, DOCK6, ANTXR1, CCM2, ENG, GDF2, GNAQ, KCNK3, KDR, SMAD4, MAP3K3, PDCD10, PIK3CA, PTEN , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
100 %
Uveal melanoma and blue nevi (frequent somatic mutations at codon 209 of GNAQ gene).

By CGC Genetics (Portugal).

GNAQ
Specificity
100 %
Genes
100 %
Sturge-Weber syndrome (mutation p.Arg183Gln on GNAQ gene).

By CGC Genetics (Portugal).

GNAQ
Specificity
100 %
Genes
100 %
Capillary malformations, congenital (mutation p. Arg183GIn on GNAQ gene).

By CGC Genetics (Portugal).

GNAQ
Specificity
100 %
Genes
100 %

You can get up to 34 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

ORPHANET OMIM Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NEURAL TUBE DEFECTS, FOLATE-SENSITIVE; NTDFS MONILETHRIX; MNLIX HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO