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Volumn 33, Issue 2, 1997, Pages 168-170

Foramina parietalia permagna: Report of nine cases in one family

Author keywords

foramina parietalia permagna

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHILD; DISEASE ASSOCIATION; FEMALE; HUMAN; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SKULL DEFECT; SKULL RADIOGRAPHY; SKULL SUTURE; SYNDROME DELINEATION;

EID: 0030920543     PISSN: 10344810     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1440-1754.1997.tb01023.x     Document Type: Article
Times cited : (10)

References (12)
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    • Lother K. Familiares Vorkommen von Foramina parietalia permagna. Arch. Kinderheilkd. 1959; 160: 156-68.
    • (1959) Arch. Kinderheilkd. , vol.160 , pp. 156-168
    • Lother, K.1
  • 2
    • 0025307712 scopus 로고
    • Hereditary cranium bifidum and symmetric parietal foramina are the same entity
    • Little B, Knoll KA, Klein VR, Heller KB. Hereditary cranium bifidum and symmetric parietal foramina are the same entity. Am. J. Med. Genet. 1990; 35: 453-8.
    • (1990) Am. J. Med. Genet. , vol.35 , pp. 453-458
    • Little, B.1    Knoll, K.A.2    Klein, V.R.3    Heller, K.B.4
  • 3
    • 0017096723 scopus 로고
    • Normal variants and congenital anomalies in the region of the obelion
    • Currarino G. Normal variants and congenital anomalies in the region of the obelion. Am. J. Roetgenol. 1976; 127: 487-94.
    • (1976) Am. J. Roetgenol. , vol.127 , pp. 487-494
    • Currarino, G.1
  • 5
    • 0012686248 scopus 로고
    • Observations on the process of ossification in the formation of persistent enlarged parietal foramina
    • Pendergrass EP, Pepper OHP. Observations on the process of ossification in the formation of persistent enlarged parietal foramina. Am. J. Roetgenol. 1939; 41: 343-6.
    • (1939) Am. J. Roetgenol. , vol.41 , pp. 343-346
    • Pendergrass, E.P.1    Pepper, O.H.P.2
  • 6
    • 0009871066 scopus 로고
    • Heredofamilial Deviations. Enlarged parietal foramens combined with obesity, hypogenitalism, microphthalmos and mental retardation
    • Warkany J, Weaver TS. Heredofamilial Deviations. Enlarged parietal foramens combined with obesity, hypogenitalism, microphthalmos and mental retardation. Am. J. Dis. Child. 1940; 60: 1147-54.
    • (1940) Am. J. Dis. Child. , vol.60 , pp. 1147-1154
    • Warkany, J.1    Weaver, T.S.2
  • 7
    • 0015419946 scopus 로고
    • Evolution and significance of giant parietal foramina. Report of five cases in one family
    • Fein JM, Brinker RA. Evolution and significance of giant parietal foramina. Report of five cases in one family. J. Neurosurg. 1972; 37: 487-6.
    • (1972) J. Neurosurg. , vol.37 , pp. 487-496
    • Fein, J.M.1    Brinker, R.A.2
  • 8
    • 0021277356 scopus 로고
    • Parietal foramina clavicular hypoplasia. An autosomal dominant syndrome
    • Golabi M, Carey J, Hall BD. Parietal foramina clavicular hypoplasia. An autosomal dominant syndrome. Am. J. Dis. Child. 1984; 138: 596-99.
    • (1984) Am. J. Dis. Child. , vol.138 , pp. 596-599
    • Golabi, M.1    Carey, J.2    Hall, B.D.3
  • 9
    • 70449186985 scopus 로고
    • Zur Frage der Fenestrae parietales symmetricae (sog. Foramina parietalis permagna)
    • Wiedemann HR. Zur Frage der Fenestrae parietales symmetricae (sog. Foramina parietalis permagna). Monatschr. Kinderheilk 1957; 105: 305-10.
    • (1957) Monatschr. Kinderheilk , vol.105 , pp. 305-310
    • Wiedemann, H.R.1
  • 10
    • 19144373472 scopus 로고
    • Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions on the short arm of chromosome 11
    • Bartsch O, Wuyts W, Van Hul W et al. Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions on the short arm of chromosome 11. Am. J. Hum. Genet. 1966; 58: 734-42.
    • (1966) Am. J. Hum. Genet. , vol.58 , pp. 734-742
    • Bartsch, O.1    Wuyts, W.2    Van Hul, W.3
  • 11
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    • Developmental defects in the cranial vault
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    • Lodge, T.1
  • 12
    • 0026022352 scopus 로고
    • Rare primary cranial vault and base of the skull tumors in children. Report of 30 cases with a short literature review
    • Kozlowski K, Campbell J, McAlister W et al. Rare primary cranial vault and base of the skull tumors in children. Report of 30 cases with a short literature review. La Radiologia Medica 1991; 81: 213-24.
    • (1991) La Radiologia Medica , vol.81 , pp. 213-224
    • Kozlowski, K.1    Campbell, J.2    McAlister, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.