Arthrogryposis Multiplex Congenita
Important
It is possible that the main title of the report Arthrogryposis Multiplex Congenitais not the name you expected.
Synonyms
- AMC
- Congenital Multiple Arthrogryposis
- Fibrous Ankylosis of Multiple Joints
- Multiple congenital contractures
Disorder Subdivisions
- Neurogenic Arthrogryposis Multiplex Congenita
- Myopathic Arthrogryposis Multiplex Congenita
- Guerin-Stern Syndrome
- Amyoplasia Congenita
General Discussion
Arthrogryposis Multiplex Congenita, a rare disorder that is present at birth (congenital), is characterized by reduced mobility of many joints of the body. Impairment of mobility is due to the overgrowth (proliferation) of fibrous tissue in the joints (fibrous ankylosis). There are many different types of Arthrogryposis Multiplex Congenita and the symptoms vary widely among affected individuals. In the most common form of Arthrogryposis Multiplex Congenita, the range of motion of the joints in the arms and legs (limbs) is limited or fixed. Other findings may include inward rotation of the shoulders, abnormal extension of the elbows, and bending of the wrists and fingers. In addition, the hips may be dislocated and the heels of the feet may be inwardly bent from the midline of the leg while the feet are inwardly bent at the ankle (clubfoot). The cause of Arthrogryposis Multiplex Congenita (AMC) is unknown. Most types of Arthrogryposis Multiplex Congenita are not inherited; however, a rare autosomal recessive form of the disease has been reported in one large inbred Arabic kindred in Israel.
Resources
Human Growth Foundation
997 Glen Cove Avenue
Glen Head
NY
11545
Tel: (516)671-4041
Fax: (516)671-4055
800: (800)451-6434
hgf1@hgfound.org
http://www.hgfound.org/
MAGIC Foundation for Children's Growth
6645 W. North Avenue
Oak Park
IL
60302
Tel: (708)383-0808
Fax: (708)383-0899
800: (800)362-4423
mary@magicfoundation.org
http://www.magicfoundation.org
AVENUES
P.O. Box 5192
Sonora
CA
95370
info@avenuesforamc.com
http://www.avenuesforamc.com
Arthrogryposis Group
Beak Cottage
Dunley
Stourport-on-Severn
Intl
DY13 OTZ
United Kingdom
Tel: 01747 822655
Fax: 01747 822655
taguk@aol.com
http://tagonline.org.uk
Arachnoiditis Information and Support Network
c/o Medium Chain Acyl-CoA Dehydrogenease (MCAD) Family Support Group
2345 Yonge Street, 9th Floor
Toronto
Ontario
M4P 2E5
Canada
cast@freenet.hamilton.on.caNIH/National Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse
1 AMS Circle
Bethesda
MD
20892-3675
USA
Tel: (301)495-4484
Fax: (301)718-6366
800: (877)226-4267
TDD: (301)565-2966
NIAMSinfo@mail.nih.gov
http://www.niams.nih.gov/Health_Info
MUMS (Mothers United for Moral Support, Inc) National Parent-to-Parent Network
150 Custer Court
Green Bay
WI
54301-1243
USA
Tel: (920)336-5333
Fax: (920)339-0995
800: (877)336-5333
mums@netnet.net
http://www.netnet.net/mums/
For a Complete Report:
This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
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.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email orphan@rarediseases.org
Last Updated: 4/11/2008
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WebMD Medical Reference from the National Organization of Rare Disorders
