Cerebro Oculo Facio Skeletal Syndrome
Synonyms of Cerebro Oculo Facio Skeletal Syndrome
- Cerebrooculofacioskeletal Syndrome
- Cockayne Syndrome type II
- COFS Syndrome
- Pena Shokeir II Syndrome
- Pena Shokeir Syndrome Type II
- No subdivisions found.
Cerebro-oculo-facio-skeletal (COFS) syndrome is a genetic degenerative disorder of the brain and spinal cord that begins before birth. The disorder is characterized by growth failure at birth and little or no neurological development, structural abnormalities of the eye and fixed bending of the spine and joints. Abnormalities of the skull, face, limbs and other parts of the body may also occur. COFS syndrome is inherited as an autosomal recessive genetic trait. COFS is now considered to be part of the spectrum of disorders within Cockayne syndrome.
Cerebro-oculo-facio-skeletal syndrome was first described in 1974. Symptoms of this disorder include unusual craniofacial features. These may include an extremely small head (microcephaly), an unusually prominent nose, abnormally small eyes, clouding of the eye's lens (cataract), and a horizontally narrow opening between the eyelids (blepharophimosis). The ears are abnormally large, the upper lip overlaps the lower, the groove in the upper lip (philtrum) is abnormally long, and the jaw is unusually small (micrognathia).
In most patients, fixed bending of the elbows and knees (flexion contractures), a hunched back (kyphosis), and bending of one or more fingers (camptodactyly) occurs. Infants with cerebro-oculo-facio-skeletal syndrome usually have so-called "rocker bottom" feet and a groove over the length of the soles of the feet. A deformity of the hip (coxa valga) and porous bones (osteoporosis) may also occur.
Other features of this disorder include wide-set nipples, failure to thrive, slowed growth (developmental retardation), lack of muscle tone (hypotonia), feeding difficulties and one line in the palm of the hand formed by fusion of the usual two lines (simian crease). Children with cerebro-oculo-facio-skeletal syndrome have an increased vulnerability to respiratory infections.
Individuals with COFS syndrome show progressive deterioration and rarely survive beyond seven years.
Cerebro-oculo-facio-skeletal syndrome is an autosomal recessive genetic disorder. 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. Recessive genetic disorders occur when an individual inherits the same abnormal gene for the same trait from each parent. If an individual receives one normal gene and one gene for the disease, the person will be a carrier for the disease, but usually will not show symptoms. The risk for two carrier parents to both pass the defective gene and, therefore, have an affected child is 25% with each pregnancy. The risk to have a child who is a carrier like the parents is 50% with each pregnancy. The chance for a child to receive normal genes from both parents and be genetically normal for that particular trait is 25%. The risk is the same for males and females.
All individuals carry 4-5 abnormal genes. Parents who are close relatives (consanguineous) have a higher chance than unrelated parents to both carry the same abnormal gene, which increases the risk to have children with a recessive genetic disorder.
COFS syndrome has been found to be associated with mutations in genes responsible for repairing DNA damage. These genes are called excision repair cross-complementing genes and include ERCC6, ERCC8 and ERCC2.
Cerebro-oculo-facio-skeletal syndrome is a very rare disorder present at birth. It affects males and females and occurs in many ethnic groups.
Symptoms of the following disorders can be similar to those of oculo-facio-skeletal syndrome. Comparisons may be useful for a differential diagnosis:
Neu-Laxova syndrome is an autosomal recessive genetic disorder characterized by growth retardation before birth and multiple abnormalities at birth. These abnormalities include a small head (microcephaly) and abnormal limbs, skin, external genitals and afterbirth (placenta).
Children with various features common to both COFS Syndrome and Neu-Laxova syndrome have also been described in the medical literature.
Potter syndrome (bilateral renal agenesis) is a rare condition characterized by a flattened face with a "parrot-beak" nose, wide-set eyes and abnormalities of the eyelids, unusual smallness of the jaw and low-set, floppy ears. They have more skin than necessary and it appears dehydrated. A kidney may be absent or underdeveloped. Skeletal abnormalities such as clubfeet and contracted joints occur frequently among infants with this disorder.
Seckel syndrome (bird-headed dwarfism; nanocephalic dwarfism) is an autosomal recessive genetic disorder characterized by low birth weight, an abnormally small head, mental retardation, large eyes, a large beaklike nose, a narrow face, and a receding lower jaw. Multiple deformities such as an underdeveloped thumb, dislocation of the thighbone head, clubfoot, curvature of the spine, eyes that don't look in parallel directions, and gastrointestinal abnormalities may also occur. Examination of the brain shows a simplified gross structure of the cerebrum with a relatively intact cerebellum. (For more information on this disorder, choose "Seckel" as your search term in the Rare Disease Database.)
The diagnosis of COFS syndrome is often made based on physical features seen at birth. X-ray studies may reveal displacement of the small foot bones between the ankle and toes (second metatarsals) and neuroimaging studies may show reduced white matter with gray matter mottling. DNA repair studies on skin fibroblast cells may help to confirm a diagnosis of COFS syndrome. Molecular genetic testing to identify mutations in the excision repair genes is available on a research basis only.
Treatment of COFS syndrome is symptomatic and supportive. Genetic counseling is recommended for families of children with the disorder.
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 Cerebro Oculo Facio Skeletal Syndrome
Rosser T and Pearl PL. Cerebro-Oculo-Facio-Skeletal Syndrome. In: The NORD Guide to Rare Disorders, Philadelphia: Lippincott, Williams and Wilkins, 2003: 520-521.
Jones KL. Smith's recognizable patterns of human malformation, 4th ed. Philadelphia: WB Saunders, 1998.
Graham JM, Anyan-Yeboa K, Raams A, et al. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy. Am J Hum Genet 2001;69:291-300.
Meira LB, Graham JM, Greenberg CR, et al. Manitoba aboriginal kindred with original cerebro-oculo-facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene. Am J Hum Genet 2000;66:1221-8.
Graham JR, Greenberg CR, Anyane-Yeboa K, et al. COFS syndrome caused by defective nucleotide excision repair . Am J Hum Genet 1998;63:A33.
Del Bigio MR, Greenberg CR, Rorke LB, et al. Neuropathologic findings in eight patients with cerebro-oculo-facio-skeletal (COFS) syndrome. J Neuropathol 1997;56:1147-1157.
Harden CL, Tuchman AJ, Daras M. Infantile spasms in COFS syndrome. Pediatr Neurol 1991;7:302-304.
Hwang WS, Trevenen CL, Greenberg C, et al. Chondro-osseus changes in cerebro-oculo-facial-skeletal syndrome. J Pathol 1982;138:33-40.
FROM THE INTERNET
McKusick VA, ed. Online Mendelian Inheritance in Man (OMIM). Baltimore, MD: The Johns Hopkins University Press; Entry No. 214150; Last Update: 9/20/01.
Nance MA , (updated 15 October 2001). Cockayne Syndrome In: GeneReviews at GeneTests: Medical Genetics Information Resource (database online). Copyright, University of Washington, Seattle. 1997-2003. Available at http://www.genetests.org Accessed 8/03.
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 ©1988, 1989, 1996, 2003
Report last updated: 2008/02/28 00:00:00 GMT+0
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.