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Genetics Home Reference: your guide to understanding genetic conditions
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Juvenile hyaline fibromatosis

Reviewed December 2008

What is juvenile hyaline fibromatosis?

Juvenile hyaline fibromatosis is a disorder that affects the skin, joints, and bones. Individuals with this condition typically begin to develop signs and symptoms within the first few years of life. Juvenile hyaline fibromatosis is characterized by skin bumps that frequently appear on the hands, neck, scalp, ears, and nose. These skin bumps can also develop in joint creases and the genital region. They vary in size and are sometimes painful. Affected individuals usually develop more skin bumps over time.

Juvenile hyaline fibromatosis is also characterized by overgrowth of the gums (gingival hypertrophy) and joint deformities (contractures) that can impair movement. In addition, affected individuals may grow slowly and have bone abnormalities. People with juvenile hyaline fibromatosis typically have severe physical limitations, but most individuals have normal intelligence and live into adulthood.

How common is juvenile hyaline fibromatosis?

The prevalence of juvenile hyaline fibromatosis is unknown. About 70 people with this disorder have been reported.

What genes are related to juvenile hyaline fibromatosis?

Mutations in the ANTXR2 gene (also known as the CMG2 gene) cause juvenile hyaline fibromatosis. The ANTXR2 gene provides instructions for making a protein involved in the formation of tiny blood vessels (capillaries). Researchers believe that the ANTXR2 protein is also important for maintaining the structure of basement membranes, which are thin, sheet-like structures that separate and support cells in many tissues.

The signs and symptoms of juvenile hyaline fibromatosis are caused by the accumulation of a clear (hyaline) substance in different parts of the body. The nature of this substance is not well known, but it is likely made up of protein and sugar molecules. Researchers suspect that mutations in the ANTXR2 gene disrupt the formation of basement membranes, allowing the hyaline substance to leak through and build up in various body tissues.

Related Gene(s)

Changes in this gene are associated with juvenile hyaline fibromatosis.

  • ANTXR2

How do people inherit juvenile hyaline fibromatosis?

This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.

Where can I find information about diagnosis or management of juvenile hyaline fibromatosis?

These resources address the diagnosis or management of juvenile hyaline fibromatosis and may include treatment providers.

  • Gene Review: Hyalinosis, Inherited Systemic (http://www.ncbi.nlm.nih.gov/books/NBK1525/)
  • Genetic Testing Registry: Hyaline fibromatosis syndrome (http://www.ncbi.nlm.nih.gov/gtr/conditions/C2745948)

You might also find information on the diagnosis or management of juvenile hyaline fibromatosis in Educational resources (http://www.ghr.nlm.nih.gov/condition/juvenile-hyaline-fibromatosis/show/Educational+resources) and Patient support (http://www.ghr.nlm.nih.gov/condition/juvenile-hyaline-fibromatosis/show/Patient+support).

General information about the diagnosis (http://ghr.nlm.nih.gov/handbook/consult/diagnosis) and management (http://ghr.nlm.nih.gov/handbook/consult/treatment) of genetic conditions is available in the Handbook. Read more about genetic testing (http://ghr.nlm.nih.gov/handbook/testing), particularly the difference between clinical tests and research tests (http://ghr.nlm.nih.gov/handbook/testing/researchtesting).

To locate a healthcare provider, see How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

Where can I find additional information about juvenile hyaline fibromatosis?

You may find the following resources about juvenile hyaline fibromatosis helpful. These materials are written for the general public.

You may also be interested in these resources, which are designed for healthcare professionals and researchers.

What other names do people use for juvenile hyaline fibromatosis?

  • inherited systemic hyalinosis
  • juvenile hyalinosis
  • molluscum fibrosum
  • Murray syndrome
  • Puretic syndrome
  • Systemic hyalinosis

For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines (http://ghr.nlm.nih.gov/ConditionNameGuide) and How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.

What if I still have specific questions about juvenile hyaline fibromatosis?

Ask the Genetic and Rare Diseases Information Center (http://rarediseases.info.nih.gov/GARD/).

What glossary definitions help with understanding juvenile hyaline fibromatosis?

autosomal ; autosomal recessive ; basement membranes ; capillaries ; cell ; gene ; gingival ; gums ; hypertrophy ; inherited ; joint ; juvenile ; prevalence ; protein ; recessive ; syndrome

You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://www.ghr.nlm.nih.gov/glossary).

References

  • Antaya RJ, Cajaiba MM, Madri J, Lopez MA, Ramirez MC, Martignetti JA, Reyes-Múgica M. Juvenile hyaline fibromatosis and infantile systemic hyalinosis overlap associated with a novel mutation in capillary morphogenesis protein-2 gene. Am J Dermatopathol. 2007 Feb;29(1):99-103. (http://www.ncbi.nlm.nih.gov/pubmed/17284973?dopt=Abstract)
  • Dowling O, Difeo A, Ramirez MC, Tukel T, Narla G, Bonafe L, Kayserili H, Yuksel-Apak M, Paller AS, Norton K, Teebi AS, Grum-Tokars V, Martin GS, Davis GE, Glucksman MJ, Martignetti JA. Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis. Am J Hum Genet. 2003 Oct;73(4):957-66. Epub 2003 Sep 12. (http://www.ncbi.nlm.nih.gov/pubmed/12973667?dopt=Abstract)
  • Gene Review: Hyalinosis, Inherited Systemic (http://www.ncbi.nlm.nih.gov/books/NBK1525/)
  • Hanks S, Adams S, Douglas J, Arbour L, Atherton DJ, Balci S, Bode H, Campbell ME, Feingold M, Keser G, Kleijer W, Mancini G, McGrath JA, Muntoni F, Nanda A, Teare MD, Warman M, Pope FM, Superti-Furga A, Futreal PA, Rahman N. Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Am J Hum Genet. 2003 Oct;73(4):791-800. Epub 2003 Aug 21. (http://www.ncbi.nlm.nih.gov/pubmed/14508707?dopt=Abstract)
  • OMIM: HYALINE FIBROMATOSIS SYNDROME (http://omim.org/entry/228600)
  • Rahman N, Dunstan M, Teare MD, Hanks S, Edkins SJ, Hughes J, Bignell GR, Mancini G, Kleijer W, Campbell M, Keser G, Black C, Williams N, Arbour L, Warman M, Superti-Furga A, Futreal PA, Pope FM. The gene for juvenile hyaline fibromatosis maps to chromosome 4q21. Am J Hum Genet. 2002 Oct;71(4):975-80. Epub 2002 Sep 4. (http://www.ncbi.nlm.nih.gov/pubmed/12214284?dopt=Abstract)

 

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

 
Reviewed: December 2008
Published: July 28, 2014