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Volumn 6, Issue 1, 1997, Pages 13-19

New syndrome: Brain malformation, growth retardation, hypokinesia and polyhydramnios in two brothers

Author keywords

brain abnormalities and hypokinesia; X linked inheritance

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; CHILD; GENETIC DISORDER; GROWTH RETARDATION; HUMAN; HYDRAMNIOS; HYPOKINESIA; MALE; PRIORITY JOURNAL; SYNDROME DELINEATION; X CHROMOSOME RECESSIVE INHERITANCE;

EID: 0031028922     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (15)
  • 3
    • 0023990453 scopus 로고
    • Callosal defect, microcephaly, severe mental retardation and other anomalies in three sibs
    • da Silva EO (1988): Callosal defect, microcephaly, severe mental retardation and other anomalies in three sibs. Am J Med Gen 29: 837-843.
    • (1988) Am J Med Gen , vol.29 , pp. 837-843
    • Da Silva, E.O.1
  • 6
    • 0002253401 scopus 로고
    • Analysis of Pena Shokeir phenotype
    • Hall JG (1986): Analysis of Pena Shokeir phenotype. Am J Med Genet 25: 99-117.
    • (1986) Am J Med Genet , vol.25 , pp. 99-117
    • Hall, J.G.1
  • 7
    • 0024245673 scopus 로고
    • Microcephaly, holoprosencephaly, hypokinesia-second report of a new syndrome
    • Hockey A, Crowhurst J, Cullity G (1988): Microcephaly, holoprosencephaly, hypokinesia-second report of a new syndrome. Prenat Diagn 8: 683-686.
    • (1988) Prenat Diagn , vol.8 , pp. 683-686
    • Hockey, A.1    Crowhurst, J.2    Cullity, G.3
  • 9
    • 0022262946 scopus 로고
    • Concurrent agenesis of the corpus callosum and ureteroceles in siblings
    • Lachiewicz AM, Kogan SJ, Levitt SB, Weiner RL (1985): Concurrent agenesis of the corpus callosum and ureteroceles in siblings. Pediatrics 75: 904-907.
    • (1985) Pediatrics , vol.75 , pp. 904-907
    • Lachiewicz, A.M.1    Kogan, S.J.2    Levitt, S.B.3    Weiner, R.L.4
  • 10
    • 0024384397 scopus 로고
    • Pena-Shokeir phenotype in sibs with macrocephaly but without growth retardation
    • Lammer EJ, Donnelly S, Holmes LB (1989): Pena-Shokeir phenotype in sibs with macrocephaly but without growth retardation. Am J Med Gen 32: 478-481.
    • (1989) Am J Med Gen , vol.32 , pp. 478-481
    • Lammer, E.J.1    Donnelly, S.2    Holmes, L.B.3
  • 12
    • 0017071609 scopus 로고
    • A syndrome of ankyloses, facial anomalies and pulmonary hypoplasia secondary to fetal neuromuscular dysfunction
    • Mease AD, Jeatman GW, Pettett G, Merenstein GB (1976): A syndrome of ankyloses, facial anomalies and pulmonary hypoplasia secondary to fetal neuromuscular dysfunction. In Birth Defects Original Article Series XII (5): 193-200.
    • (1976) Birth Defects Original Article Series , vol.12 , Issue.5 , pp. 193-200
    • Mease, A.D.1    Jeatman, G.W.2    Pettett, G.3    Merenstein, G.B.4
  • 13
    • 0021694098 scopus 로고
    • Anthropometric measurements of the newborn infant 27 to 41 gestational weeks
    • 7 March of Dimes Birth Defects Foundation, White Plains, NY
    • Merlob P, Sivan Y, Reisner SH (1984): Anthropometric measurements of the newborn infant 27 to 41 gestational weeks. Birth Defects: Original Article Series, 20, 7 March of Dimes Birth Defects Foundation, White Plains, NY.
    • (1984) Birth Defects: Original Article Series , pp. 20
    • Merlob, P.1    Sivan, Y.2    Reisner, S.H.3
  • 14
    • 0023635160 scopus 로고
    • Prenatal diagnosis of a new syndrome: Holoprosencephaly with hypokinesia
    • Morse RP, Rawnsley E, Sargent SK, Graham JM Jr (1987): Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesia. Prenat Diagn 7: 631-638.
    • (1987) Prenat Diagn , vol.7 , pp. 631-638
    • Morse, R.P.1    Rawnsley, E.2    Sargent, S.K.3    Graham Jr., J.M.4
  • 15
    • 0023832842 scopus 로고
    • Prenatal sonographic diagnosis of Pena-Shokeir Syndrome Type I, or fetal akinesia deformation sequence
    • Ohlsson A, Fong KW, Rose TH, Moore DC (1988): Prenatal sonographic diagnosis of Pena-Shokeir Syndrome Type I, or fetal akinesia deformation sequence. Am J Med Genet 29: 59-65.
    • (1988) Am J Med Genet , vol.29 , pp. 59-65
    • Ohlsson, A.1    Fong, K.W.2    Rose, T.H.3    Moore, D.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.