Cutis Marmorata Telangiectatica Congenita

National Organization for Rare Disorders, Inc.

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It is possible that the main title of the report Cutis Marmorata Telangiectatica Congenita is not the name you expected.

Disorder Subdivisions

  • None

General Discussion

Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital (present at birth)disorder characterized by discolored patches of skin caused by widened (dilated) surface blood vessels. As a result, the skin has a purple or blue "marbled" or "fishnet" appearance (cutis marmorata). In some affected individuals, ulcerations or congenital skin defects (aplasia cutis) can be present. The latter association can be part of Adams-Oliver syndrome. Additional associated abnormalities have been reported including pink or dark red, irregularly shaped patches of skin (nevus flammeus); loss of muscle tissue (wasting) on one side of the body (hemiatrophy); elevated fluid pressure within the eye (glaucoma); and/or undergrowth (hypotrophy) of one leg. However, many if not all of those cases represent forms of Klippel-Trenaunay syndrome or related disorders, in particular Cowden's disease. The most common association of true CMTC is with soft tissue (subcutaneous fat and muscle) hypoplasia. The disorder formerly known as macrocephaly-cutis marmoratatelangiectatica congenital (M-CMTC) is a distinct genetic disease and is now called macrocephaly-capillary malformation (M-CM/MCAP) Virtually all cases of CMTC occur randomly for no apparent reason (sporadically). It is thought that CMTC represents a form of genetic mosaicism.

Supporting Organizations

CMTC-OVM Cutis Marmorata Telangiectatica

Bitterschoten 15
Leusdan, 3831 PC
The Netherlands
Tel: 31334946671
Email: president@cmtc.nl
Website: http://www.cmtc.nl

CMTC-OVM US

3715 Wesley Chapel Rd.
Zanesville, OH 43701
Email: president@cmtcovm-us.org
Website: http://www.cmtcovm-us.org/

Canadian CMTC Foundation

645 Hayden Cres
Cobourg, Ontario K9A 2V4
Canada
Website: http://www.canadiancmtcfoundation.com/

Cobalamin Network

P.O. Box 174
Thetford Center, VT 05075-0174
USA
Tel: (802)785-4029
Email: suebee18@valley.net

Genetic and Rare Diseases (GARD) Information Center

PO Box 8126
Gaithersburg, MD 20898-8126
Tel: (301)251-4925
Fax: (301)251-4911
Tel: (888)205-2311
Website: http://rarediseases.info.nih.gov/GARD/

Hemihypertrophy Support

4581 Magnolia Dr.
Suffolk, VA 23435
Tel: (757)615-3686
Email: hemihypertrophy@yahoogroups.com

March of Dimes

1275 Mamaroneck Avenue
White Plains, NY 10605
Tel: (914)997-4488
Fax: (914)997-4763
Email: AskUs@marchofdimes.org or preguntas@nacersano.org
Website: http://www.marchofdimes.org and nacersano.org

NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases

Information Clearinghouse
One AMS Circle
Bethesda, MD 20892-3675
USA
Tel: (301)495-4484
Fax: (301)718-6366
Tel: (877)226-4267
Email: NIAMSinfo@mail.nih.gov
Website: http://www.niams.nih.gov/

National Organization of Vascular Anomalies

PO Box 38216
Greensboro, NC 27438-8216
Email: khall@novanews.org
Website: http://www.novanews.org

Nevus Network

PO Box 305
West Salem, NC 44287
USA
Tel: (419)853-4525
Fax: (405)377-3403
Email: info@nevusnetwork.org
Website: http://www.nevusnetwork.org/

The Arc

1825 K Street NW, Suite 1200
Washington, DC 20006
Tel: (202)534-3700
Fax: (202)534-3731
Tel: (800)433-5255
Email: info@thearc.org
Website: http://www.thearc.org

Vascular Birthmarks Foundation

P.O. Box 106
Latham, NY 12110
USA
Tel: (877)823-4646
Email: vbfpresident@gmail.com
Website: http://www.birthmark.org

For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders (NORD). For a full-text version of this report, go to www.rarediseases.org and click on Rare Disease Database under "Rare Disease Information".

The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only.

It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.

This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.

Last Updated:  7/10/2015
Copyright  2015 National Organization for Rare Disorders, Inc.