Hennekam syndrome;Syndrome de Hennekam

Archives de Pediatrie

Volumn 5, Issue 12, 1998, Pages 1344-1346

  Erkan, T ^a,b   Kutlu, T ^a   Cullu F ^a   Celik M ^a   Demir, T ^a   Tuysuz B ^a   Tumay G T ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

^b Vi nezade Mah Kireçhane Sok   (Turkey)

Author keywords

Abnormalities; Child; Edema; Lymphangiectasis; Protein losing enteropathies

Indexed keywords

ALPHA 1 ANTITRYPSIN; HUMAN ALBUMIN; IRON; MEDIUM CHAIN TRIACYLGLYCEROL;

ARTICLE; CASE REPORT; CHILD; EDEMA; ENTERIC FEEDING; FACE MALFORMATION; FEMALE; HEMANGIOMA; HUMAN; HYPOGAMMAGLOBULINEMIA; HYPOPROTEINEMIA; INTESTINE LYMPHANGIECTASIA; IRON DEFICIENCY ANEMIA; MENTAL DEFICIENCY; SYNDROME;

EID: 0032406879     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0929-693X(99)80054-2     Document Type: Article

References (13)

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2. 2 Waldmann TA. Protein-losing enteropathy. Gastroenterology 1966 ; 50 : 422-43
3. 3 Vardy PA, Lebenthal E, Shwachman H. Intestinal lymphangiectasia: a reappraisal. Pediatrics 1975 ; 55 : 842-51
4. 4 Strober W, Wochner RD, Carbone PP, Waldmann TA. Intestinal tymphangiectasia: a protein-losing enteropathy with hypogammaglobulinemia, lymphocytopenia, and impaired homograft rejection. J Clin Invest 1967 ; 46 : 1643-56
5. 5 Hennekam RCM, Geerdink RA, Hamel BCJ, Hennekam FAM, Kraus P, Rammeloo JA et al. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation. Am J Med Genet 1989 ; 34 : 593-600
6. 6 Gabrielli O, Catassi C, Carlucci A, Coppa GV, Giorgi P. Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: confirmation of the Hennekam syndrome. Am J Med Genet 1991 ; 40 : 244-7
7. 7 Yasunaga M, Yamanaka C, Mayumi M, Momoi T, Mikawa H. Protein-losing gastroenteropathy with facial anomaly and growth retardation: a mild case of Hennekam syndrome. Am J Med Genet 1993 ; 45 : 477-80
8. 8 Cormier-Daire V, Lyonnet S, Lehnert A, Martin D, Salomon R, Patey N et al. Craniosynostosis and kidney malformation in a case of Hennekam syndrome. Am J Med Genet 1995 ; 57 : 66-8
9. 9 Angle B, Hersh JH. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations. Am J Med Genet 1997 ; 71 : 211-4
10. 10 Rosen FS, Smith DH, Earle R, Janeway CA, Gitlin D. The etiology of hypoproteinemia in a patient with congenital chylous ascites. Pediatrics 1962 ; 30 : 696-706
11. 11 Van der Putte SC. The development of the lymphatic system in man. Adv Anat Embryol Cell Biol 1975 ; 51 : 3-60
12. 12 Opitz JM. On congenital lymphedema [editorial]. Am J Med Genet 1986 ; 24 : 127-9
13. 13 Lewis JM, Wald ER. Lymphedema praecox. J Pediatr 1984 ; 104 : 641-8