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Volumn 11, Issue 4, 2002, Pages 297-298

Spontaneous chylothorax in a case of cardio-facio-cutaneous syndrome

Author keywords

Cardio facio cutaneous syndrome; Spontaneous chylothorax

Indexed keywords

ARTICLE; CARDIOFACIOCUTANEOUS SYNDROME; CASE REPORT; CHYLOTHORAX; CRYPTORCHISM; EVOKED VISUAL RESPONSE; HUMAN; HYPERTELORISM; INFANT; KARYOTYPE 46,XY; LYMPHATIC SYSTEM DISEASE; MACROGLOSSIA; MALE; NOONAN SYNDROME; PRIORITY JOURNAL; RESPIRATORY DISTRESS;

EID: 0036791086     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200210000-00014     Document Type: Article
Times cited : (5)

References (6)
  • 2
    • 0026448345 scopus 로고
    • Spontaneous chylothorax in Noonan syndrome: Treatment with prednisolone
    • Goens MB, Campbell D, Wiggins JW (1992). Spontaneous chylothorax in Noonan syndrome: treatment with prednisolone. AJDC 146:1453-1456.
    • (1992) AJDC , vol.146 , pp. 1453-1456
    • Goens, M.B.1    Campbell, D.2    Wiggins, J.W.3
  • 3
    • 0034645512 scopus 로고    scopus 로고
    • Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: Identification of a severe phenotype
    • Grebe TA, Clericuzio C (2000). Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype. Am J Med Genet 95:135-143.
    • (2000) Am J Med Genet , vol.95 , pp. 135-143
    • Grebe, T.A.1    Clericuzio, C.2
  • 4
    • 0025794320 scopus 로고
    • Editorial comment: The Noonan-CFC controversy
    • Neri G, Zollino M, Reynolds JF (1991). Editorial comment: The Noonan-CFC controversy. Am J Med Genet 39:367-370.
    • (1991) Am J Med Genet , vol.39 , pp. 367-370
    • Neri, G.1    Zollino, M.2    Reynolds, J.F.3
  • 5
    • 0034640676 scopus 로고    scopus 로고
    • Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: Identification of a candidate region for CFC syndrome
    • Rauen KA, Cotter PD, Bitts SM, Cox VA, Golabi M (2000). Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndrome. Am J Med Genet 93:219-222.
    • (2000) Am J Med Genet , vol.93 , pp. 219-222
    • Rauen, K.A.1    Cotter, P.D.2    Bitts, S.M.3    Cox, V.A.4    Golabi, M.5
  • 6
    • 0022454854 scopus 로고
    • New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement - The CFC syndrome
    • Reynolds JF, Neri G, Herrmann JP, Blumberg B, Coldwell JG, Miles PV, Opitz JM (1986). New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement - the CFC syndrome. Am J Med Genet 25:413-427.
    • (1986) Am J Med Genet , vol.25 , pp. 413-427
    • Reynolds, J.F.1    Neri, G.2    Herrmann, J.P.3    Blumberg, B.4    Coldwell, J.G.5    Miles, P.V.6    Opitz, J.M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.