메뉴 건너뛰기




Volumn 14, Issue 2, 2005, Pages 101-103

Severe feeding difficulties in 3C syndrome

Author keywords

3C syndrome; Congenital cardiac defects; Dysmorphic facial feature; Malformation of the brain

Indexed keywords

3C SYNDROME; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CEREBELLUM DISEASE; CLINICAL FEATURE; CONGENITAL HEART DISEASE; CRANIOFACIAL MALFORMATION; DANDY WALKER SYNDROME; FEEDING DISORDER; FEMALE; GASTROESOPHAGEAL REFLUX; GROWTH DISORDER; HUMAN; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SKULL MALFORMATION;

EID: 16444367017     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200504000-00010     Document Type: Article
Times cited : (4)

References (10)
  • 1
    • 0026583129 scopus 로고
    • An additional patient with the 3C syndrome
    • Gurrieri F, Neri G (1992). An additional patient with the 3C syndrome. Clin Genet 41:263-265.
    • (1992) Clin Genet , vol.41 , pp. 263-265
    • Gurrieri, F.1    Neri, G.2
  • 2
    • 0028023704 scopus 로고
    • 3C (cranio-cerebello-cardiac syndrome: A recently delineated and easily recognizable congenital malformation syndrome
    • Hoo JJ, Kreiter M, Halverson N, Perszyk A (1994). 3C (cranio-cerebello- cardiac syndrome: a recently delineated and easily recognizable congenital malformation syndrome. Am J Med Genet 52:66-69.
    • (1994) Am J Med Genet , vol.52 , pp. 66-69
    • Hoo, J.J.1    Kreiter, M.2    Halverson, N.3    Perszyk, A.4
  • 3
    • 0031028433 scopus 로고    scopus 로고
    • Ritscher-Schinzel (3C) syndrome: Documentation of the phenotype
    • Kosaki K, Curry CJ, Roeder E, Jones KL (1997). Ritscher-Schinzel (3C) Syndrome: Documentation of the Phenotype. Am J Med Genet 68:421-427.
    • (1997) Am J Med Genet , vol.68 , pp. 421-427
    • Kosaki, K.1    Curry, C.J.2    Roeder, E.3    Jones, K.L.4
  • 4
    • 0035882375 scopus 로고    scopus 로고
    • Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: Report of four new cases and review
    • Leonardi ML, Pai GS, Wilkes B, Lebel RR (2001). Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review. Am J Med Genet 102:237-242.
    • (2001) Am J Med Genet , vol.102 , pp. 237-242
    • Leonardi, M.L.1    Pai, G.S.2    Wilkes, B.3    Lebel, R.R.4
  • 7
    • 0022889651 scopus 로고
    • Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: A new syndrome?
    • Ritscher D, Schinzel A, Boltshauser E, Briner J, Arbenz U, Sigg P (1987). Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome? Am J Med Genet 26: 481-491.
    • (1987) Am J Med Genet , vol.26 , pp. 481-491
    • Ritscher, D.1    Schinzel, A.2    Boltshauser, E.3    Briner, J.4    Arbenz, U.5    Sigg, P.6
  • 9
    • 0024521568 scopus 로고
    • 3C syndrome - Third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome)
    • Verloes A, Dresse MF, Jovanovic M, Dodinval P, Geubelle F (1989). 3C syndrome - third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome). Clin Genet 35:205-208.
    • (1989) Clin Genet , vol.35 , pp. 205-208
    • Verloes, A.1    Dresse, M.F.2    Jovanovic, M.3    Dodinval, P.4    Geubelle, F.5
  • 10
    • 0033527767 scopus 로고    scopus 로고
    • The 3C syndrome: Evolution of the phenotype and growth hormone deficiency
    • Wheeler PG, Sadeghi-Nejad A, Elias ER (1999). The 3C syndrome: evolution of the phenotype and growth hormone deficiency. Am J Med Genet 87:61-64.
    • (1999) Am J Med Genet , vol.87 , pp. 61-64
    • Wheeler, P.G.1    Sadeghi-Nejad, A.2    Elias, E.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.