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Volumn 20, Issue 1, 2011, Pages 32-37

Cantu syndrome and lymphoedema

Author keywords

Cantu syndrome; congenital generalized hypertrichosis; heterochromia iridis; lymphoedema

Indexed keywords

ADULT; AORTA VALVE REGURGITATION; ARTICLE; BRONCHOSPASM; CANTU SYNDROME; CARDIOMEGALY; CASE REPORT; CHILD; CLINICAL ASSESSMENT; CLINODACTYLY; DIASTOLIC DYSFUNCTION; ESTHETIC SURGERY; FACE ASYMMETRY; FACE DYSMORPHIA; FEMALE; HALLUX VALGUS; HEART LEFT VENTRICLE HYPERTROPHY; HEART VENTRICLE HYPERTROPHY; HETEROCHROMIA IRIDIS; HUMAN; HYPERTRICHOSIS; IRIS DISEASE; LONG PHILTRUM; LYMPH VESSEL; LYMPHATIC DRAINAGE; LYMPHEDEMA; MACROCEPHALY; PATENT DUCTUS ARTERIOSUS; PRESCHOOL CHILD; PRIORITY JOURNAL; PUBERTY; PULMONARY VALVE STENOSIS; SYNDROME;

EID: 78650789392     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e32833d015c     Document Type: Article
Times cited : (20)

References (7)
  • 1
    • 0020052574 scopus 로고
    • A distinct osteochondrodysplasia with hypertrichosis-individualization of a probable autosomal recessive entity
    • Cantu JM, Garcia-Cruz D, Sanchez-Corona J, Hernandez A, Nazara Z (1982). A distinct osteochondrodysplasia with hypertrichosis-individualization of a probable autosomal recessive entity. Hum Genet 60:36-41.
    • (1982) Hum Genet , vol.60 , pp. 36-41
    • Cantu, J.M.1    Garcia-Cruz, D.2    Sanchez-Corona, J.3    Hernandez, A.4    Nazara, Z.5
  • 2
    • 0020562965 scopus 로고
    • Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy
    • Dahlberg PJ, Borer WZ, Newcomer KL, Yutuc WR (1983). Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy. Am J Med Genet 16:99-104.
    • (1983) Am J Med Genet , vol.16 , pp. 99-104
    • Dahlberg, P.J.1    Borer, W.Z.2    Newcomer, K.L.3    Yutuc, W.R.4
  • 4
    • 33746601799 scopus 로고    scopus 로고
    • Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestation
    • Grange DK, Lorch SM, Cole PL, Singh GK (2006). Cantu syndrome in a woman and her two daughters: further confirmation of autosomal dominant inheritance and review of the cardiac manifestation. Am J Med Genet 140A:1673-1680.
    • (2006) Am J Med Genet , vol.140 A , pp. 1673-1680
    • Grange, D.K.1    Lorch, S.M.2    Cole, P.L.3    Singh, G.K.4
  • 6
    • 78650791973 scopus 로고    scopus 로고
    • Online Mendelian Inheritance in Man, OMIM (TM). World Wide Web URL
    • Online Mendelian Inheritance in Man, OMIM (TM) (2010). World Wide Web URL: http://www3.ncbi.nlm.nih.gov/omim.
    • (2010)
  • 7
    • 0027330323 scopus 로고
    • Persistence of Mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies
    • Urioste M, Rodriguez JI, Barcia JM, Martin M, Escriba R, Pardo M, et al. (1993). Persistence of Mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies. Am J Med Genet 47:494-503.
    • (1993) Am J Med Genet , vol.47 , pp. 494-503
    • Urioste, M.1    Rodriguez, J.I.2    Barcia, J.M.3    Martin, M.4    Escriba, R.5    Pardo, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.