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Titolo:
Diffuse mesangial sclerosis: association with unreported congenital anomalies and placental enlargement
Autore:
Mildenberger, E; Lennert, T; Kunze, J; Jandeck, C; Waldherr, R; Versmold, H;
Indirizzi:
Free Univ Berlin, Klinikum Benjamin Franklin, Dept Paediat, D-12200 Berlin, Free Univ Berlin Berlin Germany D-12200 n, Dept Paediat, D-12200 Berlin, Freein,iv Berlin, Klinikum Benjamin Franklin, Dept Ophthalmol, D-12200 Berl Free Univ Berlin Berlin Germany D-12200 n, Dept Ophthalmol, D-12200 Berl Humboldtanyiv, Fak Med, Virchow Klinikum, Dept Paediat, D-1040 Berlin, Germ Humboldt Univ Berlin Germany D-1040 m, Dept Paediat, D-1040 Berlin, Germ Gemeinschaftspraxis Pathol, Heidelberg, Germany Gemeinschaftspraxis Pathol Heidelberg Germany thol, Heidelberg, Germany
Titolo Testata:
ACTA PAEDIATRICA
fascicolo: 12, volume: 87, anno: 1998,
pagine: 1301 - 1303
SICI:
0803-5253(199812)87:12<1301:DMSAWU>2.0.ZU;2-U
Fonte:
ISI
Lingua:
ENG
Soggetto:
NEPHROTIC SYNDROME;
Keywords:
congenital nephrotic syndrome; diffuse mesangial sclerosis; Galloway-Mowat syndrome; placental enlargement;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
15
Recensione:
Indirizzi per estratti:
Indirizzo: Mildenberger, E Free30,iv Berlin, Klinikum Benjamin Franklin, Dept Paediat, Hindenburgdamm Free Univ Berlin Hindenburgdamm 30 Berlin Germany D-12200
Citazione:
E. Mildenberger et al., "Diffuse mesangial sclerosis: association with unreported congenital anomalies and placental enlargement", ACT PAEDIAT, 87(12), 1998, pp. 1301-1303

Abstract

A case of diffuse mesangial sclerosis (DMS) associated with a number of undescribed congenital anomalies is reported. The occurrence of additional anomalies, especially ocular anomalies, is a common finding in DMS. However, neither megalocornea, Dandy-Walker malformation, postaxial hexadactyly, rocker-bottom feet, nor atrial septal defect, as observed in our patient, has been reported previously in association with DMS. This case might be considered an atypical manifestation of the Galloway-Mowat syndrome. In contrast to most cases of DMS, the patient revealed intrauterine proteinuria as the placenta was enlarged to 31% of birth weight. This case demonstrates that the large placenta, >25% of birth weight, is not only pathognomonic of the congenital nephrotic syndrome of the Finnish type but can also occur in DMS.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/11/20 alle ore 02:04:30