Metaphyseal Chondrodysplasia, Schmid Type
NORD is very grateful to Michael Briggs, MD, Senior Research Fellow and Reader in Genetics, Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, for assistance in the preparation of this report.
Synonyms of Metaphyseal Chondrodysplasia, Schmid Type
- Japanese type spondylometaphyseal dysplasia
- Schmid metaphyseal dysostosis
- No subdivisions found.
Metaphyseal chondrodysplasia, Schmid type (MCDS), is a very rare inherited disorder characterized by short stature with abnormally short arms and legs (short-limbed dwarfism) and bowed legs (genu varum). Other physical characteristics may include outward "flaring" of the bones of the lower rib cage, lumbar lordosis, pain in the legs, and/or hip deformities in which the thigh bone is angled toward the center of the body (coxa vara). Such abnormalities of the legs and hips typically result in an unusual "waddling" walk (gait). MCDS is transmitted as an autosomal dominant trait.
In MCDS, portions of the bones of the arms and legs develop abnormally with unusual cartilage formations and subsequent abnormal bone formation at the large end portions (metaphyses) of the long bones. Bone growth normally takes place at the metaphyses, but in individuals with MCDS, the growth plate does not function as well as normal and the bones of the leg bow. Consequently, affected individuals exhibit unusually short arms and legs and short stature (short-limbed dwarfism) that usually become apparent by the second year of life.
Symptoms of MCDS are usually noticed for the first time when an infant begins walking. The legs are bowed (genu varum) and a waddling gait is present. Moderate short stature becomes apparent as the child grows. Affected children may also exhibit a hip deformity in which the thigh bone is angled toward the center of the body (coxa vara), flaring of the bones of the lower rib cage, and/or a small chest (thorax).
In some cases, affected children may experience pain in the legs, pain of the joints (arthritis), and joint stiffness. Joint pain may worsen with age.
MCDS is caused by a mutation of the gene for type X collagen called COL10A1. This gene has been mapped to chromosome 6q21-22.3. MCDS is transmitted as an autosomal dominant trait.
Chromosomes, which are present in the nucleus of human cells, carry the genetic information for each individual. Human body cells normally have 46 chromosomes. Pairs of human chromosomes are numbered from 1 through 22 and the sex chromosomes are designated X and Y. Males have one X and one Y chromosome and females have two X chromosomes. Each chromosome has a short arm designated "p" and a long arm designated "q". Chromosomes are further sub-divided into many bands that are numbered. For example, "chromosome 6q21-22.3" refers to band 21-22.3 on the long arm of chromosome 6. The numbered bands specify the location of the thousands of genes that are present on each chromosome.
Genetic diseases are determined by the combination of genes for a particular trait that are on the chromosomes received from the father and the mother.
Dominant genetic disorders occur when only a single copy of an abnormal gene is necessary for the appearance of the disease. The abnormal gene can be inherited from either parent, or can be the result of a new mutation (gene change) in the affected individual. The risk of passing the abnormal gene from affected parent to offspring is 50% for each pregnancy regardless of the sex of the resulting child.
Metaphyseal chondrodysplasia Schmid type is a very rare bone disorder that affects males and females in equal numbers. Individuals of several large families (kindred) have been documented in the medical literature.
Symptoms of the following disorders can be similar to those of Schmid type metaphyseal chondrodysplasia. Comparisons may be useful for differential diagnosis:
McKusick type metaphyseal chondrodysplasia, also known as cartilage-hair hypoplasia, is an extremely rare inherited disorder characterized by unusually fine, sparse hair and abnormal development of the cartilage and subsequent bone formation in the long bones of the arms and legs (metaphyseal chondrodysplasia), resulting in unusually short arms and legs and short stature (short-limbed dwarfism). Most affected individuals exhibit impairment of certain white blood cells (T-cells) that play an important role in helping the body's immune system fight certain infections (cellular immunodeficiency). In addition, affected individuals may also exhibit impaired absorption of certain necessary nutrients (malabsorption); abnormally low levels of certain white blood cells in the body (neutropenia and lymphocytopenia); low levels of circulating red blood cells (anemia); increased susceptibility to repeated infections, such as chickenpox; abnormalities of the teeth; and/or other physical findings. The range and severity of symptoms vary widely from case to case. McKusick type metaphyseal chondrodysplasia is inherited as an autosomal recessive genetic trait. (For more information on this disorder, choose "McKusick type metaphyseal chondrodysplasia" as your search term in the Rare Disease Database.)
Jansen type metaphyseal chondrodysplasia is an extremely rare inherited disorder characterized by severe short stature with abnormally short arms and legs (short-limbed dwarfism). Abnormally short arms and legs result from the improper formation of the cartilage at the end portions (metaphyses) of the long bones (metaphyseal chondrodysplasia). Improper cartilage development may also occur in the metaphyses of other bones of the body, particularly those of the hands and feet (i.e., metacarpals and metatarsals). Affected children may also exhibit malformation of certain bones of the skull; deformities of certain joints including swelling, pain, and stiffness; abnormally short fingers (brachydactyly); and/or abnormal front-to-back and side-to-side curvature of the spine (kyphoscoliosis). In addition, affected children may have abnormally high levels of calcium in the blood (hypercalcemia). Jansen type metaphyseal chondrodysplasia is thought to be inherited as an autosomal dominant genetic trait. (For more information on this disorder choose, "Jansen yype metaphyseal chondrodysplasia " as your search term in the Rare Disease Database.)
Spahr type metaphyseal chondrodysplasia is an extremely rare inherited disorder characterized by abnormal development of the cartilage and subsequent bone formation in the long bones of the arms and legs (metaphyseal chondrodysplasia), resulting in severely bowed legs and short stature (short-limbed dwarfism). This disorder is very similar to Schmid type metaphyseal chondrodysplasia except Spahr type metaphyseal chondrodysplasia is thought to be inherited as an autosomal recessive genetic trait.
Vitamin D deficiency rickets is a rare inherited disorder characterized by skeletal abnormalities due, in most cases, to a deficiency in vitamin D levels (Type I) or inability to properly utilize vitamin D (Type II). Skeletal abnormalities may include bowed legs; abnormal front-to-back and side-to-side curvature of the spine (kyphoscoliosis); malformations of the bones of the spine, pelvis, and legs; and/or, in severe cases, abnormal side-to-side (horizontal) depression of the lower portion of the chest cavity (Harrison Groove). In most cases, affected infants will exhibit abnormally low levels of calcium in the blood (hypocalcemia). (For more information on this disorder, choose "rickets, vitamin D deficiency" as your search term in the Rare Disease Database.)
In most cases, the diagnosis of MCDS is suspected during early childhood, usually by the second or third year of life. The diagnosis may be confirmed by a thorough clinical evaluation, identification of characteristic physical findings, and a variety of specialized tests, particularly advanced imaging techniques. These techniques include x-ray studies that may reveal abnormal development of the large (bulbous) ends (metaphyses) of certain bones of the body, particularly those of the arms and legs, abnormal enlargement of the growing end of the upper portion of the thigh bone (capital femoral epiphysis).
Molecular genetic testing for the COL10A1 gene is available to confirm the diagnosis. This test involves sequence of DNA from the COL10A1 gene and should detect any disease causing mutations. Prenatal diagnosis is available if the specific COL10A1 mutation has been identified in the family.
MCDS is often mistaken for vitamin D deficiency rickets. It is important that proper diagnosis is made as to avoid unnecessary and potentially harmful vitamin D therapy.
The treatment of MCDS is directed toward the specific symptoms that are apparent in each individual. Treatment may require the coordinated efforts of a team of specialists. Pediatricians, orthopedic surgeons, physical therapists, and other health care professionals may need to systematically and comprehensively plan an affected child's treatment.
Physical therapy and/or orthopedic surgery may help correct certain specific findings associated with metaphyseal chondrodysplasia, Schmid type, such as deformity of the hip.
Early intervention is important to ensure that children with MCDS reach their potential. Special services that may be beneficial to affected children may include speech therapy, special social support, physical therapy, and other medical, social, and/or vocational services.
Growth hormone therapy is not effective to increase final adult height.
Genetic counseling will be of benefit for affected individuals and their families. Other treatment for this disorder is symptomatic and supportive.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Organizations related to Metaphyseal Chondrodysplasia, Schmid Type
Savariarayan R. Schmid Metaphyseal Chondrodysplasia. In: The NORD Guide to Rare Disorders. Philadelphia: Lippincott, Williams and Wilkins; 2003:248.
Royce PM, Steinmann B. Connective Tissue and Its Heritable Disorders. 2nd ed. New York, NY: Wiley-Liss, Inc.;. 2002:919-20.
Beers MH, Berkow R., eds. The Merck Manual, 17th ed. Whitehouse Station, NJ: Merck Research Laboratories; 1999:2412.
Jones KL. ed. Smith's Recognizable Patterns of Human Malformation. 5th ed. Philadelphia, PA : W. B. Saunders Co.; 1997:382-86.
Kanazawa H, Tanaka H, Inoue M, et al. Efficacy of growth hormone therapy for patients with skeletal dysplasia. J Bone Miner Metab. 2003;21:307-10.
Nishimura G, Manabe N, Kosaki K, et al. Spondylar dysplasia in type X collagenopathy. Pediatr Radiol. 2001;31:76-80.
Savarirayan R, Cormier-Daire V, Lachman RS, et al. Schmid type metaphyseal chondrodysplasia: a spondylometaphyseal dysplasia identical to the "Japanese" type. Pediatr Radiol. 2000;30:460-63.
Matsui Y, Yasui N, Kawabata H, et al. A novel type X collagen gene mutation (G595R) associate with Schmid-type metaphyseal chondrodysplasia. J Hum Genet. 2000;45:105-08.
Ikegawa S, Nishimura G, Nagai T, et al. Mutation of the type X collagen gene (COL10A1) causes spondylometaphyseal dysplasia. Am J Hum Genet. 1998;63:1659-62.
Olsen BR. Mutations in collagen genes resulting in metaphyseal and epiphyseal dysplasias. Bone. 1995;17(2 Suppl):45S-49S.
Chen H. Skeletal Dysplasia. Emedicine. http://emedicine.medscape.com/article/943343-overview. Updated August 11, 2011. Accessed February 23, 2012.
Online Mendelian Inheritance in Man (OMIM). The Johns Hopkins University. Metaphyseal Chondrodysplasia, Schmid Type; MCDS. Entry No: 156500. Last Edited February 3, 2011. Available at: http://www.ncbi.nlm.nih.gov/omim/. Accessed February 23, 2012.
Online Mendelian Inheritance in Man (OMIM). The Johns Hopkins University. Collagen, Type X, Alpha-1; COL10A1. Entry No: 120110. Last Edited February 3, 2011. Available at: http://www.ncbi.nlm.nih.gov/omim/. Accessed February 23, 2012.
The information in NORD’s Rare Disease Database is for educational purposes only. It should never be used for diagnostic or treatment purposes. If you have questions regarding a medical condition, always seek the advice of your physician or other qualified health professional. NORD’s reports provide a brief overview of rare diseases. For more specific information, we encourage you to contact your personal physician or the agencies listed as “Resources” on this report.
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
Copyright ©1993, 1997, 2005, 2009, 2012
Report last updated: 2012/03/16 00:00:00 GMT+0
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.