190 related articles for article (PubMed ID: 10946350)
1. Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's report.
Jacquemont S; Barbarot S; Bocéno M; Stalder JF; David A
Am J Med Genet; 2000 Aug; 93(4):264-8. PubMed ID: 10946350
[TBL] [Abstract][Full Text] [Related]
2. Hennekam syndrome presenting as nonimmune hydrops fetalis, congenital chylothorax, and congenital pulmonary lymphangiectasia.
Bellini C; Mazzella M; Arioni C; Campisi C; Taddei G; Tomà P; Boccardo F; Hennekam RC; Serra G
Am J Med Genet A; 2003 Jul; 120A(1):92-6. PubMed ID: 12794699
[TBL] [Abstract][Full Text] [Related]
3. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
Hennekam RC; Geerdink RA; Hamel BC; Hennekam FA; Kraus P; Rammeloo JA; Tillemans AA
Am J Med Genet; 1989 Dec; 34(4):593-600. PubMed ID: 2624276
[TBL] [Abstract][Full Text] [Related]
4. Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review.
Van Balkom ID; Alders M; Allanson J; Bellini C; Frank U; De Jong G; Kolbe I; Lacombe D; Rockson S; Rowe P; Wijburg F; Hennekam RC
Am J Med Genet; 2002 Nov; 112(4):412-21. PubMed ID: 12376947
[TBL] [Abstract][Full Text] [Related]
5. Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.
de Bruyn G; Casaer A; Devolder K; Van Acker G; Logghe H; Devriendt K; Cornette L
Eur J Pediatr; 2012 Mar; 171(3):447-50. PubMed ID: 21918810
[TBL] [Abstract][Full Text] [Related]
6. Possible new autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes.
Irons MB; Bianchi DW; Geggel RL; Marx GR; Bhan I
Am J Med Genet; 1996 Dec; 66(1):69-71. PubMed ID: 8957515
[TBL] [Abstract][Full Text] [Related]
7. Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype.
Forzano F; Faravelli F; Loy A; Di Rocco M
Am J Med Genet; 2002 Jul; 111(1):68-70. PubMed ID: 12124738
[TBL] [Abstract][Full Text] [Related]
8. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
Angle B; Hersh JH
Am J Med Genet; 1997 Aug; 71(2):211-4. PubMed ID: 9217224
[TBL] [Abstract][Full Text] [Related]
9. Craniosynostosis and kidney malformation in a case of Hennekam syndrome.
Cormier-Daire V; Lyonnet S; Lehnert A; Martin D; Salomon R; Patey N; Broyer M; Ricour C; Munnich A
Am J Med Genet; 1995 May; 57(1):66-8. PubMed ID: 7645602
[TBL] [Abstract][Full Text] [Related]
10. Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: confirmation of the Hennekam syndrome.
Gabrielli O; Catassi C; Carlucci A; Coppa GV; Giorgi P
Am J Med Genet; 1991 Aug; 40(2):244-7. PubMed ID: 1897580
[TBL] [Abstract][Full Text] [Related]
11. Familial congenital non-immune hydrops, chylothorax, and pulmonary lymphangiectasia.
Stevenson DA; Pysher TJ; Ward RM; Carey JC
Am J Med Genet A; 2006 Feb; 140(4):368-72. PubMed ID: 16419129
[TBL] [Abstract][Full Text] [Related]
12. Congenital pulmonary lymphangiectasis with chylothorax: a heterogeneous lymphatic vessel abnormality.
Moerman P; Vandenberghe K; Devlieger H; Van Hole C; Fryns JP; Lauweryns JM
Am J Med Genet; 1993 Aug; 47(1):54-8. PubMed ID: 8368253
[TBL] [Abstract][Full Text] [Related]
13. [Hennekam syndrome: a case report and review of literature].
Zhang N; Shen WB; Cai HC; Yan XM; Liu SL; Wu D; Sun G; Qian JM; Dun ZN; Zhao YQ
Zhonghua Nei Ke Za Zhi; 2013 Mar; 52(3):192-6. PubMed ID: 23856108
[TBL] [Abstract][Full Text] [Related]
14. Familial non-immune hydrops fetalis and congenital pulmonary lymphangiectasia.
Njølstad PR; Reigstad H; Westby J; Espeland A
Eur J Pediatr; 1998 Jun; 157(6):498-501. PubMed ID: 9667408
[TBL] [Abstract][Full Text] [Related]
15. [Syndrome of left heart hypoplasia, causing hydrops fetalis and congenital pulmonary lymphangiectasis].
Herranz Jordán B; Campo Sampedro F; Cabezas Segurado F; Martínez Tallo EM; Galán Goméz E; Cardesa García JJ
An Esp Pediatr; 1988 Jul; 29(1):65-7. PubMed ID: 3190008
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
Fotiou E; Martin-Almedina S; Simpson MA; Lin S; Gordon K; Brice G; Atton G; Jeffery I; Rees DC; Mignot C; Vogt J; Homfray T; Snyder MP; Rockson SG; Jeffery S; Mortimer PS; Mansour S; Ostergaard P
Nat Commun; 2015 Sep; 6():8085. PubMed ID: 26333996
[TBL] [Abstract][Full Text] [Related]
17. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
Terespolsky D; Farrell SA; Siegel-Bartelt J; Weksberg R
Am J Med Genet; 1995 Nov; 59(3):329-33. PubMed ID: 8599356
[TBL] [Abstract][Full Text] [Related]
18. Bilateral congenital glaucoma in a child with hydrops fetalis, congenital pulmonary lymphangiectasia, and lymphoedema.
Haugen OH; Krohn J
J Pediatr Ophthalmol Strabismus; 2000; 37(1):44-6. PubMed ID: 10714695
[No Abstract] [Full Text] [Related]
19. Congenital pulmonary lymphangiectasia: an unusual presentation of nonimmune hydrops in a preterm infant.
Mele P; Sridhar S
Adv Neonatal Care; 2012 Jun; 12(3):166-71. PubMed ID: 22668688
[TBL] [Abstract][Full Text] [Related]
20. Multimodal imaging in the congenital pulmonary lymphangiectasia-congenital chylothorax-hydrops fetalis continuum.
Bellini C; Mazzella M; Campisi C; Taddei G; Mosca F; Tomà P; Villa G; Boccardo F; Sementa AR; Hennekam RC; Serra G
Lymphology; 2004 Mar; 37(1):22-30. PubMed ID: 15109074
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]