Document Detail


Craniosynostosis.
MedLine Citation:
PMID:  9092279     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Primary craniosynostosis, the premature closure of one or more cranial sutures, occurs in up to one in 2,500 births. Secondary causes of craniosynostosis include disorders that lead to failure of brain development and conditions that influence bone metabolism. The craniosynostoses result in skull deformities and increased intracranial pressure as the developing brain is compressed. Clinical signs and symptoms depend on which suture or combination of sutures are involved. The etiology of craniosynostosis is believed to concern genetic abnormalities in fibroblast growth factors or their receptors, and the craniosynostoses can be associated with other congenital syndromes. The most important differential diagnoses are molding that occurs during birth in young infants, and positional molding that occurs as a result of excessive time spent in the supine position in older infants. The diagnosis may be confirmed by plain films of the skull, and surgical treatment is usually indicated to prevent neurologic complications.
Authors:
F L McIntyre
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  American family physician     Volume:  55     ISSN:  0002-838X     ISO Abbreviation:  Am Fam Physician     Publication Date:  1997 Mar 
Date Detail:
Created Date:  1997-04-04     Completed Date:  1997-04-04     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  1272646     Medline TA:  Am Fam Physician     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1173-8     Citation Subset:  AIM; IM    
Affiliation:
Cape Cod Hospital, Hyannis, Massachusetts, USA.
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MeSH Terms
Descriptor/Qualifier:
Adult
Craniosynostoses* / classification,  diagnosis,  etiology,  therapy
Diagnosis, Differential
Female
Humans

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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