Hennekam syndrome presenting as nonimmune hydrops fetalis, congenital chylothorax, and congenital pulmonary lymphangiectasia

被引:34
作者
Bellini, C
Mazzella, M
Arioni, C
Campisi, C
Taddei, G
Tomà, P
Boccardo, F
Hennekam, RC
Serra, G
机构
[1] Univ Genoa, Dipartimento Pediat, Ist Giannina Gaslini, Serv Patol Neonatale,DIPE, I-16147 Genoa, Italy
[2] Univ Genoa, DISCAT, I-16147 Genoa, Italy
[3] Univ Genoa, Dipartimento Med Interna, DIMI, I-16147 Genoa, Italy
[4] Ist Giannina Gaslini, Serv Radiol, I-16148 Genoa, Italy
[5] Univ Amsterdam, Acad Med Ctr, Dept Pediat Clin Genet, NL-1105 AZ Amsterdam, Netherlands
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2003年 / 120A卷 / 01期
关键词
Hennekam syndrome; nonimmune hydrops fetalis; chylothorax; pulmonary lymphangiectasia;
D O I
10.1002/ajmg.a.20180
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report a female infant with congenital lymphedema, facial anomalies, intestinal lymphangiectasia consistent with a diagnosis of Hennekam syndrome. At birth the patient presented with severe respiratory distress due to nonimmune hydrops fetalis, a congenital chylothorax (CC), and pulmonary lymphangiectasia. Hydrops fetalis may be present in newborns with the Hennekam syndrome. Lymphoscintigraphy can be useful in explaining pleural-pulmonary involvement of this generalized lymph vessel malformation syndrome. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:92 / 96
页数:5
相关论文
共 25 条
[1]  
Angle B, 1997, AM J MED GENET, V71, P211, DOI 10.1002/(SICI)1096-8628(19970808)71:2<211::AID-AJMG17>3.3.CO
[2]  
2-E
[3]   Lymphoscintigraphic evaluation of congenital lymphedema of the newborn [J].
Bellini, C ;
Arioni, C ;
Mazzella, M ;
Campisi, C ;
Taddei, G ;
Boccardo, F ;
Serra, G .
CLINICAL NUCLEAR MEDICINE, 2002, 27 (05) :383-384
[4]  
BELLINI C, 2002, ITAL J PEDIAT, V28, P61
[5]   Children with congenital pulmonary lymphangiectasia: After infancy [J].
Chung, CJ ;
Fordham, LA ;
Barker, P ;
Cooper, LL .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1999, 173 (06) :1583-1588
[6]   CRANIOSYNOSTOSIS AND KIDNEY MALFORMATION IN A CASE OF HENNEKAM SYNDROME [J].
CORMIERDAIRE, V ;
LYONNET, S ;
LEHNERT, A ;
MARTIN, D ;
SALOMON, R ;
PATEY, N ;
BROYER, M ;
RICOUR, C ;
MUNNICH, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 57 (01) :66-68
[7]   Hennekam syndrome [J].
Erkan, T ;
Kutlu, T ;
Çullu, F ;
Çelik, M ;
Demir, T ;
Tüysüz, B ;
Tümay, GT .
ARCHIVES DE PEDIATRIE, 1998, 5 (12) :1344-1346
[8]   Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: Further case of Hennekam syndrome with a severe phenotype [J].
Forzano, F ;
Faravelli, F ;
Loy, A ;
Di Rocco, M .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 111 (01) :68-70
[9]   INTESTINAL LYMPHANGIECTASIA, LYMPHEDEMA, MENTAL-RETARDATION, AND TYPICAL FACE - CONFIRMATION OF THE HENNEKAM SYNDROME [J].
GABRIELLI, O ;
CATASSI, C ;
CARLUCCI, A ;
COPPA, GV ;
GIORGI, P .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 40 (02) :244-247
[10]  
Gilewski MK, 1996, AM J MED GENET, V66, P438