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X-linked myopathy with excessive autophagy (XMEA) is an extremely rare genetic disorder characterized by muscle disease (myopathy). The disorder is fully expressed in males only and is characterized by slowly progressive muscle weakness, especially in the legs. Onset is usually during childhood often between 5-10 years of age. XMEA occurs due to mutations of an unidentified gene on the X chromosome. The disorder is inherited an X-linked recessive trait.
The symptoms of XMEA usually become apparent during childhood. The disorder is fully expressed in males only. Females who carry the defective gene do not develop any apparent symptoms (asymptomatic) or only very mild symptoms.
The key finding in XMEA is slowly progressive muscle weakness, especially of the proximal muscles of the legs. The proximal muscles are those closer to the center of the body (e.g., upper leg muscles). As the disease progresses, some individuals may experience difficulty performing certain activities such as climbing stairs and running. During the second decade of life, muscles of the upper limbs or shoulders may become involved. In some cases, the muscles farther from the center of the body (distal muscles) such as those of the hands and feet may become involved.
During adulthood, muscle degeneration (atrophy) may occur. By the sixth decade of life, some individuals may need a wheelchair. According to the medical literature, XMEA is not associated with involvement of other organ systems.
XMEA is inherited as an X-linked recessive disorder. X-linked recessive genetic disorders are conditions caused by an abnormal gene on the X chromosome.
Females have two X chromosomes but one of the X chromosmomes is "turned off" and all of the genes on that chromosome are inactivated. Females who have a disease gene present on one of their X chromosomes are carriers for that disorder. Carrier females usually do not display symptoms of the disorder because it is usually the X chromosome with the abnormal gene that is "turned off." A male has one X chromosome and if he inherits an X chromosome that contains a disease gene, he will develop the disease. Males with X-linked disorders pass the disease gene to all of their daughters, who will be carriers. A male cannot pass an X-linked gene to his sons because males always pass their Y chromosome instead of their X chromosome to male offspring. Female carriers of an X-linked disorder have a 25% chance with each pregnancy to have a carrier daughter like themselves, a 25% chance to have a non-carrier daughter, a 25% chance to have a son affected with the disease, and a 25% chance to have an unaffected son.
Investigators have determined that XMEA occurs due to disruption or changes (mutations) to an unidentified gene located on the long arm (q) of the X chromosome (Xq28). Chromosomes, which are present in the nucleus of human cells, carry the genetic information for each individual. Pairs of human chromosomes are numbered from 1 through 22, and an additional 23rd pair of sex chromosomes which include one X and one Y chromosome in males and two X chromosomes in females. 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 Xq28" refers to band 28 on the long arm of the X chromosome. The numbered bands specify the location of the hundreds of genes that are present on each chromosome.
Unlike similar muscle disorders, XMEA rarely shows death (necrosis) of muscle tissue when studied under a microscope. However, the muscle tissue of individuals with XMEA does show excessive autophagy. Autophagy is a normal process in which components of a cell are broken down by that cell and reused, often during times of stress or starvation. Autophagy also plays a role in defending the body against foreign or invading substances, serving a second line of defense after the immune system. Although individuals with XMEA show excessive autophagy in muscle tissue, the exact role or significance of this finding in relationship to the development and progression of the disease is unknown.
XMEA has only been reported in approximately 20 families. It is fully expressed in males only, although females may develop mild symptoms. Because this disorder is often unrecognized, it may go undiagnosed making it difficult to determine its true frequency in the general population.
XMEA was first described in the medical literature in 1988.
Symptoms of the following disorders can be similar to those of XMEA. Comparisons may be useful for a differential diagnosis.
Danon disease is a rare genetic multisystem disorder characterized by the triad of muscle disease (myopathy), abnormal thickening of the walls of the heart resulting in obstruction of blood flow in and out of the heart (hypertrophic cardiomyopathy), and, in some cases, mild mental retardation. The disorder is fully expressed in males only, although females may experience some symptoms, especially heart abnormalities. In some cases, heart abnormalities may result in life-threatening complications. Muscle disease in Danon disease is similar to that found in XMEA. Danon disease is inherited as an X-linked trait. A gene responsible for the disorder has been located on the long arm (q) of the X chromosome (Xq24). (For more information on this disorder, choose Danon as your search term in the Rare Disease Database.)
Emery-Dreifuss muscular dystrophy is a rare, often slowly progressive form of muscular dystrophy affecting the muscles of the arms, legs, face, neck, spine and heart. The disorder consists of the clinical triad of weakness and degeneration (atrophy) of certain muscles, joints that are fixed in a flexed or extended position (contractures), and abnormalities affecting the heart (cardiomyopathy). Major symptoms may include muscle wasting and weakness particularly in the upper legs and arms (humeroperoneal regions) and contractures of the elbows, Achilles tendons, and upper back muscles. In some cases, additional abnormalities may be present. Emery-Dreifuss muscular dystrophy is inherited as an X-linked, autosomal dominant or autosomal recessive trait. (For more information on this disorder, choose "Emery Dreifuss" as your search term in the Rare Disease Database.)
Limb-girdle muscular dystrophy is a group of rare muscle disorders. At least 10 different disorders are included in this group. In most cases, the muscles around the hips and shoulder girdle are affected first. Most of these disorders are inherited as an autosomal recessive trait. The symptoms of limb-girdle muscular dystrophy usually occur during childhood or young adulthood as pelvic muscle weakness. Shoulder weakness, which may lead to loss of mobility, usually occurs over the next 20-30 years. Additional muscles may become involved as the disorder progresses. (For more information on this disorder, choose "Limb-Girdle Muscular Dystrophy" as your search term in the Rare Disease Database.)
A diagnosis of XMEA is made based upon a thorough clinical evaluation, a detailed patient history and surgical removal and microscopic evaluation (biopsy) of affected muscle tissue.
No specific therapy exists for XMEA. The treatment of XMEA is directed toward the specific symptoms that are apparent in each individual. In some cases, individuals in their sixties or older may eventually become wheelchair dependent.
Genetic counseling may be of benefit for affected individuals and their families. Other treatment is symptomatic and supportive.
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FROM THE INTERNET
Myopathy, X-linked, with excessive autophagy. Orphanet encyclopedia, June 2006. Available at: http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=25980 Accessed on: July 30, 2006.
McKusick VA., ed. Online Mendelian Inheritance in Man (OMIM). Baltimore. MD: The Johns Hopkins University; Entry No:310440; Last Update:12/16/2005. Available at: http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310440 Accessed on: July 30, 2004.
Report last updated: 2008/01/28 00:00:00 GMT+0