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         Craniosynostosis:     more books (22)
  1. Craniosynostosis: Diagnosis, Evaluation, and Management
  2. Clinical Management of Craniosynostosis (Clinics in Developmental Medicine?? ?) by Richard Hayward, Barry Jones, et all 2004-01-16
  3. Craniosynostosis - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-20
  4. The Official Parent's Sourcebook on Craniosynostosis: Updated Directory for the Internet Age by Icon Health Publications, 2003-11
  5. Craniosynostosis
  6. Scientific Foundations and Surgical Treatment of Craniosynostosis by John A., M.D. Persing, 1989-05
  7. Facial Clefts and Craniosynostosis: Principles and Management by Timothy A. Turvey DDS, Katherine W. L. Vig BDSMSFDS(RCS)DOrth, et all 1996-01-15
  8. Craniosynostosis: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Christine Kelly, 2006
  9. Endoscopic strip craniectomy: a minimally invasive treatment for early correction of craniosynostosis.: An article from: Journal of Neuroscience Nursing by Cathy C. Cartwright, David F. Jimenez, et all 2003-06-01
  10. Craniosynostosis: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005
  11. Craniosynostosis: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Brian, PhD Hoyle, 2005
  12. Shprintzen-Goldberg craniosynostosis syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amy, MS, CGC Vance, 2005
  13. Craniosynostosis: Webster's Timeline History, 1956 - 2007 by Icon Group International, 2009-07-10
  14. Early treatment best for skull abnormalities. (Rule Out Craniosynostosis First).: An article from: Pediatric News by Norra MacReady, 2003-03-01

41. MedlinePlus Medical Encyclopedia: Craniosynostosis
craniosynostosis. abnormally shaped skull. Causes, incidence, and risk factors Return to top. The cause of craniosynostosis is unknown.
http://www.nlm.nih.gov/medlineplus/ency/article/001590.htm
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Craniosynostosis
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Skull of a newborn Alternative names Return to top Premature closure of sutures Definition Return to top Craniosynostosis is a congenital (present from before birth) defect, characterized by premature closure of one or more sutures (connections between plates in the skull), which causes an abnormally shaped skull. Causes, incidence, and risk factors Return to top The cause of craniosynostosis is unknown. In an infant's head, the sutures mark the boundaries between the bony plates that make up the skull. Premature closure of these sutures stops bony growth and results in deformity of the skull. The shape of the deformity is determined by which sutures are involved. The condition may be hereditary and caused by a genetic defect, or it can occur sporadically in a family with no other affected relatives. The hereditary form often occurs in conjunction with other defects, which can cause seizures, diminished intellectual capacity, and blindness. Symptoms Return to top
  • Absence of the normal feeling of a "soft spot" (fontanelle) on the newborn's skull Disappearance of the fontanelle early A raised hard ridge along the affected sutures Unusual head shape Slow or no increase in the head size over time as the baby grows

42. HealthlinkUSA Craniosynostosis Links
Kanoodle.com. You can find craniosynostosis right now at Info.com. Click here for page 1 of craniosynostosis information from the HealthlinkUSA directory.
http://www.healthlinkusa.com/420ent.htm

43. HealthlinkUSA Craniosynostosis Links
Thursday May 13, 2004. The healthy way to search today s best sites. Links to websites which may include treatment, cures, diagnosis
http://www.healthlinkusa.com/420.asp

44. NeurosurgeryToday.org | What Is Neurosurgery | Patient Education Materials | Cra
craniosynostosis is a congenital deformity of the infant skull that results when the skull sutures (fibrous joints) between various skull bones fuse improperly
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... Professional Information: AANS.ORG Site Map View Printer Friendly Patient Resources Adult Onset Hydrocephalus Anatomy of the Brain Anatomy of the Spine Brain Metastasis ... Tumors Craniosynostosis and Craniofacial Disorders March, 1999 Craniosynostosis is a congenital deformity of the infant skull that results when the skull sutures (fibrous joints) between various skull bones fuse improperly. Skull growth is limited at the fused suture, and growth at the remaining sutures results in an abnormal shape to the infant skull. Craniosynostosis is usually apparent in infancy and is characterized by an abnormal but characteristic head shape, depending upon how many, and which, sutures are involved. In most cases, the problem is solely cosmetic and leads to an abnormal head shape; sometimes, the growth of the facial bones is affected as well. Rarely is the growth of the skull restricted enough to cause increased pressure in the head and lead to headaches, visual loss, or developmental delays. The severity of the deformity depends on which sutures close, the point in the development process that the closure occurred, and the success or failure of the other sutures to compensate by expansion.

45. Classification Of Previously Unclassified Cases Of Craniosynostosis
Classification of previously unclassified cases of craniosynostosis. Key Words * craniosynostosis * complex disease * cranial suture.
http://www.neurosurgery.org/journals/online_j/dec96/1-6-p1.html
Classification of previously unclassified cases of craniosynostosis
Paul D. Chumas, F.R.C.S.(SN), Giuseppe Cinalli, M.D., Eric Arnaud, M.D., Daniel Marchac, M.D., and Dominique Renier, M.D. Cases of craniosynostosis usually fall into well-demarcated categories: those related to a syndrome or identified by a combination of suture involvement and morphological appearance. Between 1976 and 1995, 53 (3.6%) of 1474 cases in the craniofacial databank were assessed and designated as nonsyndromic but unclassifiable. The records and radiological studies obtained in these patients were retrospectively analyzed and comparisons were made with patients classified in the databank as having simple craniosynostoses. "Two-suture synostosis" is a relatively straightforward condition and is treatable with standard craniosynostosis techniques. However, possibly as a result of surgical compromise when two sutures are involved, the rate of reoperation is far higher than in simple suture cases. In contrast, patients in the "complex" group presenting with severe multisuture involvement require a more tailor-made approach to their management that often entails a second procedure. Key Words * craniosynostosis * complex disease * cranial suture The classification of craniosynostoses depends on a combination of criteria: 1) whether the sutural disease is part of a syndrome; 2) the morphological appearance of the patient; 3) the actual sutures involved; and 4) progression of the disease over time.[1] Using these criteria, it is possible to classify the vast majority of craniosynostoses. In a minority of cases the initial classification proves to be incorrect and other features indicating a more complex nature become apparent. It is thus necessary to have a sufficient follow-up period to be confident that the initial diagnosis still holds.

46. Craniosynostosis Q & A
craniosynostosis Q A. What is craniosynostosis? Most cases are sporadic, although there are several genetic syndromes with craniosynostosis.
http://www.neurosurgery.org/pubpages/patres/faq_cranio.html
  • What is craniosynostosis? Answer: Craniosynostosis is a congenital anomaly characterized by the premature closure of one or more cranial sutures (the fibrous joints between the bones of the skull). The disorder results in an abnormal skull and head shape. Most cases are sporadic, although there are several genetic syndromes with craniosynostosis. Disorders of the fibroblast growth factor receptor molecule have been recently found in some cases of hereditary craniosynostosis.
  • What are the symptoms of craniosynostosis? Answer: Most children with craniosynostosis do not have any symptoms; the head shape is abnormal, and the face may be malformed in certain cases. Rarely, symptoms of increased pressure in the head such as headaches, decreased appetite, vomiting, or even developmental delays or mental retardation may occur.
  • How does a craniofacial anomaly occur? Answer: Five separate bones make up the cranium of the head: the occipital bone (back portion of the skull); two parietal bones (on either side of the skull); and two frontal bones (front portion of the skull). The bones, which are in place by the 5th month of gestation, are like pieces of a puzzle, and are initially separated by sutures (or fibrous joints). The skull bones, coupled with the sutures, form a protective shield for the brain. As the brain grows, the sutures allow the skull to expand rapidly. If for any reason one or more of the sutures closes too early, the skull grows in a different direction where the bones are not resisting growth, thereby resulting in skull deformities.
  • 47. Craniosynostosis / Craniofacial Anomaly - Plastic Surgery Health Guide
    Definition, causes, diagnosing and treatments of craniosynostosis / craniofacial anomaly. Plastic Surgery. craniosynostosis (Craniofacial Anomaly).
    http://www.umm.edu/plassurg/cranio.htm

    Plastic Surgery
    Overview of Plastic Surgery... Cosmetic Plastic Surgery... Reconstructive Plastic Surgery... ... Index
    Related Resources Within UMM Plastic Surgery Plastic Surgery
    Craniosynostosis (Craniofacial Anomaly)
    Other conditions in which craniofacial anomalies may occur: Apert's Syndrome - The head usually appears short in the front and back and may be pointed at the top. Other characteristics may include webbed fingers and toes, widely spaced and protruding eyes, and dental crowding. Carpenter Syndrome - This syndrome typically includes traits such as abnormally short fingers, webbed toes, extra toes, underdeveloped jaw, highly arched palate, widely spaced eyes, and/or low-set, deformed ears. Half of patients with Carpenter syndrome also have heart defects. Cleft Palate / Cleft Lip - The incomplete closure of the lip and/or the roof of the mouth results in this defect. Crouzon's Syndrome - Characterized by abnormalities in the skull and facial bones, this syndrome often causes the skull to be short in the front and the back. Flat cheek bones and a flat nose are also typical of this disorder. Pfeiffer Syndrome - This rare disorder is characterized by abnormalities of the skull, hands, and feet.

    48. Craniosynostosis
    craniosynostosis. Some forms of craniosynostosis are associated with syndromes of multiple congenital (cranial and noncranial) anomalies.
    http://uscneurosurgery.com/glossary/c/craniosynostosis.htm

    49. UAB Health System | Craniosynostosis (Craniofacial Anomaly)
    craniosynostosis (Craniofacial Anomaly). Other conditions in which craniofacial anomalies may occur Apert s webbed. What is craniosynostosis?
    http://www.health.uab.edu/show.asp?durki=18576&site=785&return=18559

    50. Craniosynostosis - Information / Diagnosis / Treatment / Prevention
    home musculoskeletal disorders congenital anomalies craniosynostosis craniosynostosis. Information • Diagnosis • Treatment • Prevention.
    http://www.healthcyclopedia.com/musculoskeletal-disorders/congenital-anomalies/c

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    Related Topics: Support Groups Medical Definition: University of Newcastle-upon-Tyne Medical Dictionary: "craniosynostosis" Health News: Search millions of published articles for news on Craniosynostosis Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. Web Directory: Asher's Craniosynostosis Home Page Describes a family's experience with CS. Includes information and links about the condition and its treatment. Brynne and Craniosynostosis Personal experiences of a family and a child born with craniosynstosis.

    51. AllRefer Health - Craniosynostosis (Premature Closure Of Sutures)
    craniosynostosis (Premature Closure of Sutures) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs
    http://health.allrefer.com/health/craniosynostosis-info.html
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    Alternate Names : Premature Closure of Sutures Definition Craniosynostosis is a congenital (present from before birth) defect, characterized by premature closure of one or more sutures (connections between plates in the skull), which causes an abnormally shaped skull.
    Skull of a Newborn The cause of craniosynostosis is unknown. In an infant's head, the sutures mark the boundaries between the bony plates that make up the skull. Premature closure of these sutures stops bony growth and results in deformity of the skull. The shape of the deformity is determined by which sutures are involved. The condition may be hereditary and caused by a genetic defect, or it can occur sporadically in a family with no other affected relatives. The hereditary form often occurs in conjunction with other defects, which can cause seizures, diminished intellectual capacity, and blindness.

    52. Craniosynostosis.Info
    craniosynostosis refers to the early (premature) fusion of the sutures of the bone of the skull. craniosynostosis.Info. Definition
    http://www.plagiocephaly.org/cranio.htm
    Related Kelly Webworks BioAnth Web MedAnth Web Torticollis Kids ... Plagiocephaly.org Web Directory About Home Find a Physician Search by Location Search by Name Recommend a Physician brachycephaly ... neurogenic cephalic disorders [off site link to the NINDS (USA) Insurance Policy Links News Links Other Online Resources ... Head Shape Info Resources Support the Site
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    All About Plagiocephaly ... CranioChat Related Links plagiocefalia.com Sponsors Cranial Technologies Kelly Webworks KM Kelly, PhD Craniosynostosis.Info Definition:
    An infant's skull is made up of several free-floating bones connected by fibrous regions called sutures . These flexible connections allow the infant's head to pass through the birth canal and enable the skull to grow in response to the brain.
    Craniosynostosis
    refers to the early (premature) fusion of the sutures of the bone of the skull. Premature fusing of the sutures restricts and distorts the growth of the skull. These cranial growth restrictions often results in increased cranial pressure growth which can cause vision problems and impede intellectual development. In addition, abnormal head shape is associated with low self-esteem and behavioral problems. Correction of these deformities can relieve cranial pressure and in the long-term, improve the child's self-esteem.

    53. CCDD: Craniosynostosis
    The Center for Craniofacial Development and Disorders (CCDD), at Johns Hopkins University, has a comprehensive list of craniosynostosis links and articles.
    http://www.hopkinsmedicine.org/craniofacial/Gateway/Craniosynostosis.cfm
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    Craniosynostosis
    A variety of conditions in which the bones of the skull join together too early, affecting the development and shape of the skull. Craniosynostosis may occur alone or as part of a genetic syndrome. Visit these Craniosynostosis links to learn more:
    • About Us: Craniosynostosis Brochure - Craniosynostosis is defined as the premature closing of one or more of the spaces that are normally present between individual bones of the skull. Infants born with abnormal skull shapes should be evaluated for craniosynostosis. Some abnormal skull shapes at birth may be related to fetal head position and not premature fusion of sutures; this type of deformity will usually correct itself in several months.
      Family: Joan Richtsmeier Shares Her Story
      - In the case of craniosynostosis involving the sagittal suture, the brain compensates for its inability to expand upward by growing more toward the front and back, elongating the forehead and the back of the head.

    54. CCDD: Family: Education: Descriptions Of Disorders: Craniosynostosis
    Incidence craniosynostosis occurs approximately 1 in 3000 births. The most obvious manifestations of craniosynostosis is an alteration of head shape.
    http://www.hopkinsmedicine.org/craniofacial/Education/Article.cfm?ArticleID=64&S

    55. Craniosynostosis -- Topic Overview
    craniosynostosis Topic Overview What is craniosynostosis? What causes craniosynostosis? The causes of craniosynostosis are not fully understood.
    http://my.webmd.com/hw/health_guide_atoz/hw180327.asp
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    You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... Credits Craniosynostosis Topic Overview
    What is craniosynostosis?
    Craniosynostosis (craniostenosis) is a condition in which one or more sutures of a fetus's or baby's skull close prematurely and the bony plates fuse too early. As a result, the affected area of the skull does not expand normally as the brain grows, causing a misshapen head. In severe cases, usually when craniosynostosis affects more than one suture, pressure builds on the brain and may cause long-term complications. Craniosynostosis is among one of the most common physical deformities of a fetus or newborn, occurring in about 1 in every 2,000 to 2,500 births.
    What are the symptoms?

    56. Craniosynostosis
    craniosynostosis. What is craniosynostosis? The normal skull consists of several plates of bone that are separated by sutures. What causes craniosynostosis?
    http://www.chw.org/display/PPF/DocID/1810/router.asp
    Site Index Anatomy of the Newborn Skull Overview of Craniofacial Anomalies The Craniofacial Team ... Craniofacial Anomalies : Craniosynostosis E-mail this page Print this page
    Craniosynostosis
    What is craniosynostosis? The normal skull consists of several plates of bone that are separated by sutures. The sutures (fibrous joints) are found between the bony plates in the head. As the infant grows and develops, the sutures close, forming a solid piece of bone, called the skull.
    Craniosynostosis is a condition in which the sutures close too early, causing problems with normal brain and skull growth. Premature closure of the sutures may also cause the pressure inside of the head to increase and the skull or facial bones to change from a normal, symmetrical appearance.
    What causes craniosynostosis? Craniosynostosis occurs in one out of 2,000 live births and affects males twice as often as females.
    Craniosynostosis is most often sporadic (occurs by chance). In some families, craniosynostosis is inherited in one of two ways:
    • autosomal recessive - Autosomal recessive means that two copies of the gene are necessary to express the condition, one inherited from each parent, who are carriers. Carrier parents have a one in four, or 25 percent, chance with each pregnancy, to have a child with craniosynostosis. Males and females are equally affected.

    57. Health Info
    Topic craniosynostosis, Back to previous page. Topic Overview What is craniosynostosis? craniosynostosis (craniostenosis
    http://www.pamf.org/health/healthinfo/index.cfm?page=article&sgml_id=hw180325

    58. Disease Directory : Musculoskeletal Disorders : Congenital Anomalies : Craniosyn
    About craniosynostosis Childrens Hospital San Diego - About craniosynostosis - Childrens Hospital San Diego, serving the communities of Chula Vista, National
    http://www.diseasedirectory.net/Musculoskeletal_Disorders/Congenital_Anomalies/C
    Wednesday, June 02, 2004 Musculoskeletal Disorders Congenital Anomalies
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    59. Craniosynostosis
    craniosynostosis Trigonocephaly. Brachycephaly. Frontal Plagiocephaly. Sagittal Synostosis (Scaphocephaly) Most common craniosynostosis form (1 in 4200 births);
    http://www.fpnotebook.com/NIC71.htm
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    60. About Craniosynostosis - Childrens Hospital San Diego
    About craniosynostosis Childrens Hospital San Diego, serving the communities of Chula Vista, National City, El Cajon, Oceanside, El Centro, Rancho Bernardo
    http://www.chsd.org/11005.cfm
    Craniofacial Services - Home Craniofacial Core Team Members Distraction Osteogenesis Resources
    About Craniosynostosis
    What is Craniosynostosis?
    • Cranio = skull Synostosis = fusion of open areas (sutures)
    premature Background sutures When a suture closes, a predictable abnormality of head shape occurs. In certain children, changes around the eyes and face may occur because of fusion of the sutures in the cranial base. When this occurs, the child often has an associated craniofacial syndrome that must be diagnosed by a skilled geneticist. Treatment The treatment of craniosynostosis is surgical. Most cases are treated because of the resulting severe aesthetic deformities. However, a small percentage of cases are associated with increases in intracranial pressure due to changes in head shape, configuration and volume. Types of Craniosynostosis Sagittal Craniosynostosis
    The most common type of single suture fusion.
    The head becomes elongated and narrowed and takes on the shape of a boat, scaphocephaly. Metopic Craniosynostosis
    The forehead portion of the skull becomes triangular in shape and the eyes become closer together (trigonocephaly).

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