Perspectives on Craniosynostosis: Sutural Biology, Some Well-known Syndromes, and Some Unusual Syndromes

被引:22
作者
Cohen, M. Michael, Jr. [1 ]
机构
[1] Dalhousie Univ, Fac Med, Dept Pediat, Halifax, NS B3H 1W2, Canada
关键词
Anatomic and genetic perspectives; basis of craniosynostosis; growth and development; suture systems; coronal ring; primary vs. secondary synostosis; Mendelian genetic patterns; molecular basis of mutations; Muenke syndrome; Pfeiffer syndrome; thanatophoric dysplasia; Carpenter syndrome; unusual syndromes with craniosynostosis; DYSPLASIA;
D O I
10.1097/SCS.0b013e318193d48d
中图分类号
R61 [外科手术学];
学科分类号
摘要
Perspectives on craniosynostosis are discussed under the following headings: sutural biology (anatomic and genetic categories of synostosis; sutures, suture systems, and types of craniosynostosis; well-known syndromes (Muenke syndrome and Pfeiffer syndrome); and unusual syndromes (thanatophoric dysplasia, Beare-Stevenson cutis gyrata syndrome, Crouzonodermoskeletal syndrome, Carpenter syndrome, Elejalde syndrome, hypomandibular faciocranial syndrome, and craniorhiny). Five of these syndromes are caused by fibroblast growth factor receptor (FGFR) mutations; one is caused by ras-like in rat brain 23 (RAB23) mutations; and three have Mendelian patterns of inheritance, but the molecular basis remains unknown to date.
引用
收藏
页码:646 / 651
页数:6
相关论文
共 19 条
[1]  
BURDI AR, 1986, CLEFT PALATE J, V23, P28
[2]  
Cohen M., 2002, Overgrowth Syndromes
[3]  
Cohen M M Jr, 1988, Am J Med Genet Suppl, V4, P99
[4]  
Cohen M. Michael Jr, 2004, P380
[5]  
Cohen MJ., 2000, CRANIOSYNOSTOSIS DIA
[6]   PFEIFFER SYNDROME UPDATE, CLINICAL SUBTYPES, AND GUIDELINES FOR DIFFERENTIAL-DIAGNOSIS [J].
COHEN, MM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (03) :300-307
[7]   SUTURAL BIOLOGY AND THE CORRELATES OF CRANIOSYNOSTOSIS [J].
COHEN, MM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (05) :581-616
[8]  
COHEN MM, 1980, W J MED, V132, P508
[9]  
Cohen MM., 1986, Craniosynostosis: Diagnosis, Evaluation, and Management
[10]  
Elejalde B R, 1977, Birth Defects Orig Artic Ser, V13, P53