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Familial case of Milroy-Meige-Nonne disease

Ouvry, P.A.; Davy, A.; Sauzeau, M.F.; Lesieur, P.

Phlebologie 39(3): 497-508

1986

ISSN/ISBN: 0031-8280
PMID: 3786423
Document Number: 275962
Milroy-Meige-Nonne's disease is an exceptional disorder. The authors give an account of a family in which 8 cases were enumerated spread over 4 generations. The clinical pictures given show lymphatic affection of varying severity. The authors take this opportunity to give short historical and anatomical reviews of the disease. Finally they describe current treatment.

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Göpel, W.; Barthelmes, W. 1970: Total vertical ocular paralysis in a case of Friedreich-Nonne-Marie spinocerebellar heredo-ataxia (case report) Zeitschrift für Arztliche Fortbildung 64(20): 1048-1051
Dhar, S.N.; Hajini, G.H. 1976: Milroy's Disease with Nephrotic Syndrome Indian Journal of Dermatology Venereology and Leprology 42(2): 80-82
Stralla-Delidjakova, M.; Nikolovska, T.; Tadzer, I.S. 1971: Simple scintigraphic screening test for diagnosis of Milroy's disease Nuclear-Medizin 10(4): 348-354
Cai, P.; Han, J.-X. 2014: Case of Meige syndrome Zhongguo Zhen Jiu 34(1): 44
Sun, L.; Li, D.-J.; Wu, J. 2014: Case of Meige syndrome Zhongguo Zhen Jiu 34(12): 1178
Von Schéele, C.; Akerstedt, A.C. 1989: Meige's or Brueghel's syndrome? a neurologic disease that is possible to treat Lakartidningen 86(43): 3676-3678
Bobyreva, S.B.; Kovalev, M.F. 1980: Familial case of marble disease Pediatriia 2: 58
Nadezhdina, M.V.; Beĭn, B.N.; Vyvodnova, V.V. 1988: A case of familial Hippel-Lindau disease Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko 2: 56-59
Iudina, G.K.; Sholomov, I.I. 2003: A familial case of Hallervorden-Spatz disease Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 103(1): 49-50
Alaev, B.A. 1983: Clinical polymorphism in a familial case of demyelinating disease Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 83(3): 24-27
Vohra, V. 1987: Pyle's disease--familial metaphyseal dysplasia--a case report Australasian Radiology 31(1): 75-78
Verger, P.; Guichard; Puyjalon 1960: Pyle's disease or familial metaphysial dysplasia (apropos of a new case) Pediatrie 15: 27-34
Gemme, G.; Ruffa, G.; Bonioli, E.; Mangiante, G. 1976: Familial mediterreanean fever (periodic disease). Description of a case Minerva Pediatrica 28(26): 1650-1653
Bianconcini, G.; Mazzali, F.; Candini, R.; Silingardi, M.; Iori, I. 1994: Celiac disease (familial) associated with sarcoidosis. Clinical case and review of the literature Minerva Medica 85(10): 541-553
Akulenko, L.V.; Nikogosian, S.O.; Zhordaniia, K.I.; Kozachenko, V.P. 1991: Clinical course of the disease in familial and non-familial forms of serous cystadenocarcinoma of the ovary Akusherstvo i Ginekologiia 9: 58-60
Fiocchi, A.; Codara, L.; Colombini, A.; Rota, M. 1983: Gianotti's disease as a case disclosing intra-familial infection by hepatitis B virus (HBV) Minerva Pediatrica 35(23-24): 1229-1234
Fantechi, V.; Lazzeri, S.; Baldoni, D.; Maranghi, P. 1993: Chondrocalcinosis or calcium pyrophosphate dihydrate (CPPD) crystal deposition disease. Report of a familial case La Radiologia Medica 85(6): 850-853
López Ramos, D.; Gabriel, R.; Cantero Perona, J.; Moreno Otero, R.; Fernández Bermejo, M.; Maté Jiménez, J. 2001: Association of MALTectomy (appendectomy and tonsillectomy) and inflammatory bowel disease: a familial case-control study Revista Espanola de Enfermedades Digestivas: Organo Oficial de la Sociedad Espanola de Patologia Digestiva 93(5): 303-314
Xie, Y.D. 1981: Uremic medullary cystic disease (familial juvenile nephronophthiasis)--an investigation of one family and pathological report of a case Zhonghua Nei Ke Za Zhi 20(1): 45-46
Arata, H.; Takashima, H. 2007: Familial prion disease (GSS, familial CJD, FFI) Nihon Rinsho. Japanese Journal of Clinical Medicine 65(8): 1433-1437