Familial nonsyndromic craniosynostosis with specific deformity of the cranium: Case report

Journal of Neurosurgery: Pediatrics

Volumn 10, Issue 6, 2012, Pages 560-564

  Shimizu, Azusa ^a   Komuro, Yuzo ^b   Miyajima, Masakazu ^c   Arai, Hajime ^c  

^a JUNTENDO UNIVERSITY SHIZUOKA HOSPITAL   (Japan)

^b JUNTENDO UNIVERSITY URAYASU HOSPITAL   (Japan)

^c JUNTENDO UNIVERSITY   (Japan)

Author keywords

Congenital anomaly; Craniosynostosis; Familial case; Gene search; Hypotelorism

Indexed keywords

ARTICLE; CASE REPORT; CHILD DEVELOPMENT; CHROMOSOME 4; CRANIECTOMY; CRANIOFACIAL SYNOSTOSIS; DNA BINDING; DNA DETERMINATION; FAMILIAL NONSYNDROMIC CRANIOSYNOSTOSIS; FGFR GENE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENETIC POLYMORPHISM; HELIX1 GENE; HELIX2 GENE; HUMAN; HYPOTELORISM; INFANT; INTELLIGENCE; LOOP GENE; MALE; PHENOTYPE; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; SKULL MALFORMATION; SKULL SUTURE; TWIST1 GENE;

CRANIAL SUTURES; CRANIOSYNOSTOSES; CRANIOTOMY; DNA COPY NUMBER VARIATIONS; GENES, DOMINANT; HUMANS; INFANT, NEWBORN; MALE; PEDIGREE; TREATMENT OUTCOME;

EID: 84870721555     PISSN: 19330707     EISSN: 19330715     Source Type: Journal    
DOI: 10.3171/2012.8.PEDS1259     Document Type: Article

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