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2. Milroy's primary congenital lymphedema in a male infant and review of the literature. Kitsiou-Tzeli S; Vrettou C; Leze E; Makrythanasis P; Kanavakis E; Willems P In Vivo; 2010; 24(3):309-14. PubMed ID: 20555004 [TBL] [Abstract][Full Text] [Related]
3. Aplasia of superficial lymphatic capillaries in hereditary and connatal lymphedema (Milroy's disease). Bollinger A; Isenring G; Franzeck UK; Brunner U Lymphology; 1983 Mar; 16(1):27-30. PubMed ID: 6843174 [TBL] [Abstract][Full Text] [Related]
11. Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema. Daniel-Spiegel E; Ghalamkarpour A; Spiegel R; Weiner E; Vikkula M; Shalev E; Shalev SA Prenat Diagn; 2005 Nov; 25(11):1015-8. PubMed ID: 16231305 [TBL] [Abstract][Full Text] [Related]
12. [Nonne-Milroy's syndrome (hereditary lymphedema type I). Report of a clinical case]. La Placa G; Andreotti M; Pradella C; Russo F; Besana R Pediatr Med Chir; 2005; 27(1-2):106-8. PubMed ID: 16922055 [TBL] [Abstract][Full Text] [Related]
14. [Lymphedema. In Ullrich-Turner syndrome it is congenital]. Butenandt O MMW Fortschr Med; 2001 Apr; 143(15):10. PubMed ID: 11349310 [No Abstract] [Full Text] [Related]
15. Lymphedema in Noonan syndrome: clues to pathogenesis and prenatal diagnosis and review of the literature. Witt DR; Hoyme HE; Zonana J; Manchester DK; Fryns JP; Stevenson JG; Curry CJ; Hall JG Am J Med Genet; 1987 Aug; 27(4):841-56. PubMed ID: 3321992 [TBL] [Abstract][Full Text] [Related]
16. Phenotypic characterization of primary lymphedema. Connell F; Brice G; Mortimer P Ann N Y Acad Sci; 2008; 1131():140-6. PubMed ID: 18519967 [TBL] [Abstract][Full Text] [Related]
17. Distichiasis-lymphedema syndrome and the Turner phenotype. Toro-Solá MA Bol Asoc Med P R; 1991 Dec; 83(12):543-4. PubMed ID: 1811607 [TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of Nonne-Milroy lymphedema. Franceschini P; Licata D; Rapello G; Guala A; Di Cara G; Franceschini D Ultrasound Obstet Gynecol; 2001 Aug; 18(2):182-3. PubMed ID: 11547763 [No Abstract] [Full Text] [Related]
20. Compound heterozygosity for a variably penetrant variant and a variant of unknown significance in FLT4 causes fully penetrant Milroy's lymphedema. Kim J; Lim SY Lymphology; 2022; 55(2):41-46. PubMed ID: 36170577 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]