Diffuse mesangial sclerosis: Association with unreported congenital anomalies and placental enlargement

Acta Paediatrica, International Journal of Paediatrics

Volumn 87, Issue 12, 1998, Pages 1301-1303

  Mildenberger, E ^a   Lennert, T ^a   Kunze, J ^a   Jandeck, C ^a   Waldherr, R ^b   Versmold, H ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b Gemeinschaftspraxis fur Pathologie   (Germany)

Author keywords

Congenital nephrotic syndrome; Diffuse mesangial sclerosis; Galloway Mowat syndrome; Placental enlargement

Indexed keywords

ARTICLE; CASE REPORT; CONGENITAL NEPHROTIC SYNDROME; DANDY WALKER SYNDROME; DISEASE ASSOCIATION; FEMALE; FINGER MALFORMATION; FOOT MALFORMATION; HEART ATRIUM SEPTUM DEFECT; HUMAN; NEWBORN; PLACENTA DISORDER; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; FATAL OUTCOME; FEMALE; HUMANS; INFANT, NEWBORN; NEPHROTIC SYNDROME; PLACENTA;

EID: 0032407298     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/080352598750031022     Document Type: Article

References (15)

1. Mendelsohn HB, Krauss M, Berant M, Lichtig C. Familial early-onset nephrotic syndrome: diffuse mesangial sclerosis. Acta Paediatr Scand 1982; 71: 753-8
2. Habib R. Nephrotic syndrome in the 1st year of life. Pediatr Nephrol 1993; 7: 347-53
3. Waldherr R. Diffuse mesangial scleroris. In: Churg J, Bernstein J, Glassock RJ, editors. Renal disease: classification and atlas of glomerular diseases. 2nd ed. New York: Igahu-Shoin, 1995: 414-5
4. Barakat AY, Khoury LA, Allam CK, Najjar SS. Diffuse mesangial sclerosis and ocular abnormalities in two siblings. Int J Pediatr Nephrol 1982; 3: 33-5
5. Beale MC, Staver DS, Kissane JM, Robson AM. Congenital glomerulosclerosis and nephrotic syndrome in 2 infants. Am J Dis Child 1979; 133: 842-5
6. Lennert T, Härtling A, Mildenberger E, Jandeck C, Lobeck H, Waldherr R, Versmold H. Augenveränderungen bei diffuser mesangialer Sklerose (DMS). Monatsschr Kinderheilkd 1997; 145: 209
7. Huttunen NP. Congenital nephrotic syndrome of Finnish type. Study of 75 patients. Arch Dis Child 1976; 51: 344-8.
8. Wiedemann HR, Kunze J, Dibbern H. Atlas der Klinischen Syndrome für Klinik und Praxis. 3. Aufl. Stuttgart: Schattauer, 1989: 442
9. Koskimies O, Sariola H, Holmberg C, Rapola J. Clinical quiz. Pediatr Nephrol 1991; 5: 433-5
10. Cooperstone BG, Friedman A, Kaplan BS. Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy. Am Med Genet 1993; 47: 250-4
11. Nielsen KF, Steffensen GK. Congenital nephrotic syndrome associated with Lowe's syndrome. Child Nephrol Urol 1990; 10: 92-5
12. Moerman P, Verbeken E, Fryns JP, Goddeeris P, Lauweryns JM. The Meckel syndrome. Pathological and cytogenetic observations in eight cases. Hum Genet 1982; 62: 240-5
13. Meinecke P, Ziegenrucker W, Peters A. Potter sequence due to renal aplasia and postaxial hexadactyly. A distinct entity? Genet Couns 1993; 4: 127-30
14. Schinzel A, Giedion A. A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs. Am J Med Genet 1978; 1: 361-75
15. Lennert T, Neumann L, Rey M, Hofstaetter C, Lobeck H, Waldherr R. Diffuse mesangial glomerulosclerosis in three families: prenatal and postnatal onset. Pediatr Nephrol 1994; 8: C77