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Craniosynostosis: more books (22)

Craniosynostosis: Diagnosis, Evaluation, and Management
Clinical Management of Craniosynostosis (Clinics in Developmental Medicine?? ?) by Richard Hayward, Barry Jones, et all 2004-01-16
Craniosynostosis - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-20
The Official Parent's Sourcebook on Craniosynostosis: Updated Directory for the Internet Age by Icon Health Publications, 2003-11
Craniosynostosis
Scientific Foundations and Surgical Treatment of Craniosynostosis by John A., M.D. Persing, 1989-05
Facial Clefts and Craniosynostosis: Principles and Management by Timothy A. Turvey DDS, Katherine W. L. Vig BDSMSFDS(RCS)DOrth, et all 1996-01-15
Craniosynostosis: An entry from Thomson Gale's Gale Encyclopedia of Children's Health: Infancy through Adolescence by Christine Kelly, 2006
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
Craniosynostosis: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Paul Johnson, 2005
Craniosynostosis: An entry from Thomson Gale's Gale Encyclopedia of Neurological Disorders by Brian, PhD Hoyle, 2005
Shprintzen-Goldberg craniosynostosis syndrome: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Amy, MS, CGC Vance, 2005
Craniosynostosis: Webster's Timeline History, 1956 - 2007 by Icon Group International, 2009-07-10
Early treatment best for skull abnormalities. (Rule Out Craniosynostosis First).: An article from: Pediatric News by Norra MacReady, 2003-03-01

lists with details

Craniosynostosis
The cranial sutures involved in craniosynostosis are depicted and the specificoccurrences discussed.
http://www.kidsplastsurg.com/craniosynostosis.html

Extractions: As an infant's brain grows, open sutures allow the skull to expand and develop a relatively normal head shape. If one or more of the sutures has closed early, it causes the skull to expand in the direction of the open sutures. This can result in an abnormal head shape. In severe cases, this condition can also cause increased pressure on the growing brain. In sagittal synostosis (scaphocephaly), the sagittal suture is closed. As a result, the infant's head does not expand in width but grows long and narrow to accommodate the growing brain. The sagittal suture is the most common single suture involved in craniosynostosis. The incidence of sagittal synostosis in the population is approximately 1 in 4200 births. Males are affected about three times as often as females.
NINDS Forwarding Page
craniosynostosis information sheet compiled by the National Institute of NeurologicalDisorders and Stroke (NINDS).
http://www.ninds.nih.gov/health_and_medical/disorders/craniosytosis_doc.htm

Extractions: NINDS has redesigned its website and the URL for the page you were seeking has changed. The new URL for this page is /disorders/craniosynostosis/craniosynostosis.htm . Please update your bookmark to this page. You will be automatically taken to this page in 5 seconds, or you can click the link to go there now.
EMedicine - Craniosynostosis : Article By Raj D Sheth, MD
craniosynostosis craniosynostosis consists of premature fusion of 1 or morecranial sutures, often resulting in an abnormal head shape.
http://www.emedicine.com/neuro/topic80.htm

Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Neurology Pediatric Neurology Last Updated: January 25, 2005 Rate this Article Email to a Colleague Synonyms and related keywords: anterior plagiocephaly, Apert syndrome, brachycephaly, Carpenter syndrome, Chotzen syndrome, Crouzon syndrome, kleeblattschädel, cloverleaf skull, oxycephaly, Pfeiffer syndrome, plagiocephaly, scaphocephaly, trigonocephaly AUTHOR INFORMATION Section 1 of 9 Author Information Introduction Clinical Differentials ... Bibliography Author: Raj D Sheth, MD , Director Comprehensive Epilepsy Program, Professor, Departments of Neurology and Pediatrics, Department of Neurology, University of Wisconsin at Madison Coauthor(s): Bermans J Iskandar, MD , Director, Associate Professor, Departments of Neurological Surgery, Pediatrics, Children's Hospital, University of Wisconsin Hospital and Clinics Raj D Sheth, MD, is a member of the following medical societies:
HotDog Express For AOL Hometown Document
Personal experiences of a family and a child born with craniosynstosis.
http://members.aol.com/cdbosworth/brynnespage.html

Extractions: The doctor told my mommy that she better watch outI'm a strong girl! I have been rolling over onto my tummy for over a month, and can push up on one hand while reaching for a toy with the other. I can almost sit up by myself, but I still wobble. Daddy helps me to stand up, and I can stay there and dance a long time. I love playing with Mommy's hair and laughing when Daddy tickles me. Chuckie can make me laugh, too! He is a great brother and even lets me hold some of his toys (sometimes). This past week, I realized that sucking on my big toe is great fun! And I had Grandma hysterical playing the No-No game! I took a long time to come into the world. Mommy was in labor for 50 hours, and pushed for 3+1/2 hours. After trying everything, the doctor helped deliver me by cesearan.
Craniosynostosis, Endoscopic Strip Craniectomy - University Health System, San A
Minimally invasive procedures to correct craniosynostosis, endoscopic stripcraniectomy, Dr. David Jimenez and Dr. Constance Barone are the pioneers in
http://www.craniosynostosis.net/

Extractions: Dr. David Jimenez and Dr. Constance Barone are the pioneers of the new minimally invasive procedures to correct craniosynostosis, Endoscopic Strip Craniectomy. Over the last eight years they have performed more than 300 craniosynostosis procedures , with excellent outcomes Children from all over the world have come to Dr. Barone and Dr. Jimenez in order to benefit from their unmatched experience in these revolutionary craniosynostosis techniques. As the pioneers of Endoscopic Strip Craniectomies they have performed the craniosynostosis procedure more than any other surgical team in the world. Their expertise in the field has been published in several medical journals and professional publications. Endoscopic Strip Craniectomy is a newer, less invasive craniosynostosis procedure that lasts approximately one hour compared to the three to seven hours of surgery required with the traditional craniosynostosis operation. Because the procedure is performed using endoscopes, patients have shorter hospital stays, decreased need for blood transfusions and significantly smaller incisions and scaring.
Craniosynostosis - June 15, 2004 - American Family Physician
Isolated sagittal synostosis is the most common type of craniosynostosis. Of themore than 150 craniosynostosis syndromes, Crouzon s disease and Apert s
http://www.aafp.org/afp/20040615/2863.html

Extractions: FIGURE 1. Sutures and fontanelles in the normal newborn skull. C ranial skeletogenesis is unique. The cranial skeleton is composed of an assortment of neural crest and mesoderm-derived cartilages and bones that have been highly modified during evolution. Cranial malformations, although uncommon, compromise not only function but also the mental well-being of the person. Recent advances in human genetics have increased our understanding of the ways particular gene perturbations produce cranial skeletal malformations. However, an abnormal head shape resulting from cranial malformations in infants continues to be a diagnostic and therapeutic challenge. Development The bones of the cranium are divided into the skull base and the calvarial vault. The growth of skull bones is driven primarily by the expanding growth of the brain. The brain grows rapidly in utero and during the first three years of life. An infant born at term has nearly 40 percent of his or her adult brain volume, and this increases to 80 percent by three years of age. Correspondingly, the size of the cranium of an infant born at term is 40 percent of adult size; by seven years, this increases to 90 percent.
Devin's Craniosynostosis Page
Devin was born with a condition called craniosynostosis (Sagittal Synostosis) and underwent surgery (craniotomy or craniectomy), at the Hospital for Sick Kids in Toronto, Canada.
http://www.geocities.com/mikayla_cutiepatootie/Devin3_cranio.html

Extractions: More specifically Devin was diagnosed with Sagittal Synostosis, which is the premature closing of the Sagittal Suture (the suture that runs front to back). Because it had fused prematurely his skull would not be able to grow properly. As the brain was developing his skull would only be able to grow where the sutures were open (the front and the back). Hence Devin's skull was growing in a boat shape - very long and narrow with a bossing forehead and back on the head. Sagittal Synostosis is the most common form and occurs in approx. 1 out of every 2000 births. There is debate as to the cause and the effects that it may have (is there pressure on the brain?), no one really knows for sure but what they do know is that it can have profound psychological effects on the individual (looking abnormal, teasing etc). And that's when we knew we had to do something, something to give Devin the best possible childhood and the best possible chance for a healthy and happy future. To us that meant proceeding with the surgery. Although we were given the choice, to us it hardly seemed like a choice, how could we opt not to have the surgery.
Craniosynostosis
craniosynostosis is a condition in which the sutures close too early, In somefamilies, craniosynostosis is inherited in one of two ways
http://www.chw.org/display/PPF/DocID/1810/router.asp

Extractions: 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.
Cleft Lip Palate Craniosynostosis Plagiocephaly Facial Anomalies Deformity Human
Craniology is dedicated to all type of facial anomaly and facial reconstructive surgery. Craniology.org has Cleft Lip Palate, craniosynostosisPlagiocephaly , Hemifacial Microsomia (HFM), Facial Anomalies, Human Skull - Plastic Surgery forum, gallery and resources.
http://www.craniology.org
Craniosynostosis
The cranial sutures involved in craniosynostosis are depicted and the specific occurrences discussed.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Parents Of Children With Craniosynostosis
Offers information and support about craniosynostosis. For families in Eastern Idaho and parts of Utah.
http://pcc2000.org.tripod.com/

Extractions: PCC was established in 2000 based in Chubbuck, Idaho. Offering services to families in Eastern Idaho and Parts of Utah. We are dedicated in offering support to Parents of Children with this condition. Assisting them in finding information, and accessing resources available to them. Please sign our Guestbook You are visitor # Last Updated Internet Explorer Users: Click here to add this page to your list of favorites
Craniosynostosis Information Page National Institute Of
craniosynostosis information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Craniosynostosis
Premature fusing of the sutures is called craniosynostosis, Children bornwith craniosynostosis may have increased pressure on the brain and vision
http://www.pedisurg.com/PtEduc/Craniosynostosis.htm

Extractions: TEXAS PEDIATRIC SURGICAL ASSOCIATES CRANIOSYNOSTOSIS What is craniofacial surgery? Craniofacial surgery is a surgical subspecialty developed by Paul Tessier thirty years ago in France. It involves surgery of the skull and face for tumors, trauma, and congenital deformities. For many years, the severity of these conditions was thought too risky for surgical intervention. Tessier, a surgeon himself, challenged this belief and began building the foundation of craniofacial surgery. In doing so, he recognized that this complex form of surgery could only be performed by a specially trained surgeon who was supported by a highly skilled team. The surgical team at Hermann Children's Hospital includes a pediatric neurosurgeon and craniofacial surgeon as well as a specialized anesthesiologist. The neurosurgeon works on the skull and the craniofacial surgeon on the face. With both areas being closely related the combined approach offers the best possible results with the highest level of safety. What is craniosynostosis?
Craniosynostosis
(832) 3257234 craniosynostosis What is craniofacial surgery? the highest level of safety. What is craniosynostosis? Diagram of skull, showing
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
FAQ About Craniosynostosis
ABOUT craniosynostosis. When is craniofacial surgery necessary? Children withcraniosynostosis, craniofacial syndromes, and positional deformities may
http://www.pedisurg.com/PtEduc/FAQ_About_Craniosynostosis.htm

Extractions: ABOUT CRANIOSYNOSTOSIS When is craniofacial surgery necessary? The surgery is necessary in an infant who has craniosynostosis when the bones of the skull fuse together, or a craniofacial syndrome which causes fusion of the bones of the head and also abnormalities of the skull and face. What is the ideal age at which a child should have surgery for craniosynostosis? Surgery should be done within the first two weeks of life on those infants born with multiple fused sutures involved. When any of the other sutures are involved, surgery is done prior to 3 months of age when a less invasive microscopic procedure can be employed. In older children, the standard approach is employed at 6 months of age. For fusion of the remaining sutures, surgery is done at six months. Will one operation be sufficient for craniosynostosis? Most children who have single suture involvement require only one surgical procedure. However, for those with multiple suture involvement and those with craniofacial abnormalities associated with the craniosynostosis, multiple procedures are necessary. What are the risks to the child in this type of surgery?
Craniofacial Group Paris-France: Management Of Anomalies Of Skull: Craniostenosi
Craniofacial Group; Management of anomalies of skull and face craniosynostosis, facial clefts, hypertelorism, tumors and trauma.
http://www.cranio-facial.org

Extractions: For 25 years, our group, comprising the specialities of craniofacial and plastic surgery, and paediatric neurosurgery, has been dealing with craniofacial anomalies. Craniofacial surgery is especially involved with treating congenital craniofacial anomalies. The first group is represented by craniosynostosis or craniostenosis, in which the cranial sutures are prematurely fused, distorting the cranial vault (oxycephaly, trigonocephaly, brachycephaly, plagiocephaly) and faciocraniosynostosis, with facial retrusion (Crouzon, Apert, Pfeiffer, and Saethre-Chozten syndromes). Facial and monobloc distraction is often used for these patients. Another group of craniofacial anomalies is represented by facial clefts with hypertelorism, nasal anomalies, palpebral colobomata, encephaloceles, and Treacher-Collins syndrome. Many of these syndromes require complex orbital surgeries, for orbital dystopia. For example, bringing the orbits together in hypertelorism (widely-spaced orbits) requires complete orbital mobilization, such as in transcranial or subcranial facial bipartition.
Pediatric Neurosurgery - Craniofacial Anomalies
A PICTORIAL guide to the anatomy and etiology of various types of craniosynostosis is available. Please see the disclaimer.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Cranioysynostosis And Positional Plagiocephaly Support, Inc.
A national non profit organization that assists families that have, or suspect their child has, craniosynostosis or Positional Plagiocephaly. Includes information about the conditions, organization details, events, doctor listings and contact details.
http://www.CAPPSkids.org

Extractions: Fredericksburg, VA 22407 CAPPSORG@aol.com WELCOME to the CAPPS Website! Craniosynostosis And Positional Plagiocephaly Support, Inc. CAPPS is a non-profit, 501 (c)(3) tax exempt organization. Click below for information on the different conditions: Help Raise Money for CAPPS NEW: GET YOUR CAPPS AWARENESS BANDS CRANIOSYNOSTOSIS POSITIONAL PLAGIOCEPHALY STATE CONTACTS AND DOCTOR LISTINGS ... CAPPS SUPPORT BOARD Click the above Logo to enter our CAPPS store for awesome items you can share with family and friend and help CAPPS raise money and awareness
Craniosynostosis And Positional Plagiocephaly Support (CAPPS)
A national non profit organization that assists families that have, or suspect their child has, craniosynostosis or Positional Plagiocephaly.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
EMedicine - Craniosynostosis : Article By Spyros Sgouros, MD, FRCS(SN)(Glasg)
craniosynostosis The term craniosynostosis refers to the premature fusion ofone or multiple cranial sutures. craniosynostosis is commonly present at
http://www.emedicine.com/med/topic2897.htm

Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Medicine, Ob/Gyn, Psychiatry, and Surgery Neurosurgery Last Updated: October 15, 2003 Rate this Article Email to a Colleague Synonyms and related keywords: craniostenosis, craniofacial dysostosis, craniofacial defect, craniofacial surgery, cranial sutures, cosmetic facial deformity, cranial deformity, cranial malformation, intracranial hypertension, abnormal skull shape, abnormal head shape, skull growth, Crouzon syndrome, Apert syndrome, Crouzon's syndrome, Apert's syndrome, scaphocephaly, sagittal synostosis, plagiocephaly, unilateral coronal synostosis, posterior plagiocephaly, lambdoid synostosis, trigonocephaly, metopic synostosis, brachycephaly, oxycephaly, turricephaly, cloverleaf skull deformity, triphyllocephaly, pansynostosis, Saethre-Chotzen syndrome, Pfeiffer syndrome, Pfeiffer's syndrome, cranial expansion, mid-face advancement, midface advancement AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Indications Relevant Anatomy And Contraindications ... Bibliography

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