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Craniosynostosis, the early fusion of skull sutures, is a serious abnormality of infancy and childhood. Because there are many forms of the condition, both isolated and syndromatic, proper diagnosis is essential before treatment could be carried out. Not only has surgical treatment advanced in recent years, but basic knowledge of sutural and molecular biology of craniosynostosis syndromes has recently come to light. Because dramatic changes have occurred in the field, particularly in molecular biology, this new edition has been rewritten and new chapters have been added on the growth of sutures, craniofacial surgery, and epidemiology and clinical correlations. The molecular basis of craniosynostosis, with emphasis on fibroblast growth receptors, and recent research on postnatal growth and the craniofacial complex, will be discussed in detail. Many new syndromes have been delineated the established conditions have been redefined. What's new in pediatrics - UpToDate The following represent additions to UpToDate from the past six months that were considered by the editors and authors to be of particular interest. The most recent What's New entries are at the top of each ... Pediatrics - Merck Manuals Professional Edition Learn about Pediatrics symptoms diagnosis and treatment in the Merck Manual. HCP and Vet versions too! ... Merck and the Merck Manuals. Merck & Co. Inc. Kenilworth NJ USA is a global healthcare leader working to ... EMedicine - Craniosynostosis : Article By Raj D Sheth MD Craniosynostosis consists of premature fusion of 1 or more cranial sutures often resulting in an abnormal head shape. It may result from a primary defect of ossification (primary craniosynostosis) or ... Craniosynostosis - American Family Physician Craniosynostosis is the premature fusion of one or more of the cranial sutures and can occur as part of a syndrome or as an isolated defect (nonsyndromic). In the past the prevalence of craniosynostosis was ... Noonan Syndrome - American Family Physician Noonan syndrome is a common genetic disorder that causes multiple congenital abnormalities and a large number of potential health conditions. Most affected individuals have characteristic facial features that evolve ... Pediatric Craniosynostosis Treatment & Management: Medical Care ... Craniosynostosis consists of premature fusion of 1 or more cranial sutures often resulting in an abnormal head shape. It may result from a primary defect of ossification (primary craniosynostosis) or ... Abnormal Labor: Diagnosis and Management GLOWM This chapter should be cited as follows: Drennan K Blackwell S et al Glob. libr. women's med. (ISSN: 1756-2228) 2008; DOI 10.3843/GLOWM.10132 ... The diagnosis of abnormal labor (dystocia) has four major ... Microcephaly in infants and children: Etiology and evaluation Stoll C. Problems in the diagnosis of fragile X syndrome in young children are still present. Am J Med Genet 2001; 100:110. Zvulunov A Weitz R Metzker A. Neurofibromatosis type 1 in childhood: evaluation of ... Diagnosis - Craniosynostosis - Mayo Clinic Craniosynostosis requires evaluation by specialists such as a pediatric neurosurgeon or plastic surgeon. Diagnosis of craniosynostosis may include: Physical exam. Your doctor will feel your baby's head for ... N. Scott Adzick MD MMM FACS FAAP - The Children's Hospital of ... N. Scott Adzick MD MMM FACS FAAP is Surgeon-in-Chief of Children's Hospital of Philadelphia and the founder and director of the Center for Fetal Diagnosis and Treatment. ... Medical School. MD - Harvard Medical ...
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