Two brothers with Hennekam syndrome and cerebral abnormalities

Clinical Dysmorphology

Volumn 9, Issue 1, 2000, Pages 21-24

  Huppke, P ^a   Christen, H J ^a   Sattler, B ^a   Hanefeld, F ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

Cerebral abnormalities; Hennekam syndrome; Lymphoedema; Mental retardation

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; DUODENUM BIOPSY; FACE MALFORMATION; HENNEKAM SYNDROME; HUMAN; INTESTINE LYMPHANGIECTASIA; LYMPHEDEMA; MALE; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; PACHYGYRIA; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0033977959     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200009010-00004     Document Type: Article

References (6)

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2. Cormier-Daire V, Lyonnet S, Lehnert A, Martin D, Salomon R, Patey N, Broer M, Ricour C, Munnich A (1995). Craniosynostosis and kidney malformations in a case of Hennekam Syndrome. Am J Med Genet 57:66-68.
3. Gabrielli O, Catassi C, Carlucci A, Coppa GV, Giorgi P (1991). Intestinal lymphangiectasia, lymphoedema, mental retardation, and typical face: confirmation of the Hennekam syndrome. Am J Med Genet 40:244-247.
4. Hennekam RCM, Geerdink RA, Hamel BCJ, Hennekam FAM, Kraus P, Rammeloo JA, Tillemans AAW (1989). Autosomal recessive intestinal lymphangiectasia and lymphoedema with facial anomalies and mental retardation. Am J Med Genet 34:593-600.
5. Witte MH, Way DL, Witte CL, Bernas M (1997). Lymphangiogenesis: mechanisms, significance and clinical implications. EXS 79:65-112.
6. Yasunaga M, Yamanaka C, Mayumi M, Momoi T, Mikawa H (1993). Protein-losing gastroenteropathy with facial anomaly and growth retardation: a mild case of Hennekam syndrome. Am J Med Genet 45:477-480.