Nephrosis and disturbances of neuronal migration in male siblings - A new hereditary disorder?

Archives of Disease in Childhood

Volumn 61, Issue 6, 1986, Pages 545-548

  Palm, L ^a   Hagerstrand I ^a   Kristoffersson, U ^a   Blennow, G ^a   Brun, A ^a   Jorgensen C ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN HETEROTOPIA; BRAIN MALFORMATION; CASE REPORT; CENTRAL NERVOUS SYSTEM; CONGENITAL DISORDER; CONGENITAL MALFORMATION; GENETIC DISORDER; HEREDITY; HUMAN; HYDROCEPHALUS; INFANT; KIDNEY; KIDNEY MALFORMATION; NEPHROTIC SYNDROME; PRIORITY JOURNAL; PROTEINURIA;

CEREBRAL VENTRICLE NEOPLASMS; CHORISTOMA; HUMANS; INFANT, NEWBORN; KIDNEY; LINKAGE (GENETICS); MALE; NEPHROSIS; SPINAL CORD; SYNDROME; X CHROMOSOME;

EID: 0022635229     PISSN: 00039888     EISSN: None     Source Type: Journal    
DOI: 10.1136/adc.61.6.545     Document Type: Article

References (8)

1. Palm, L.; Blennow, G.; Brun, A. Infantile spasms and neuronal heterotopias Acta Paediatr Scand 1986
2. Galloway, W.H.; Mowat, A.P. Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs J Med Genet 1968 10.1136/jmg.5.4.319 5 319
3. Rakic, P. Neuronal migration and contact guidance in the primate telencephalon Postgrad Med J 1978 54 25
4. Kallen, B. Errors in the differentiation of the central nervous system Birth Defects 1979 15 43 3
5. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes 6th ed 1983 McKusick, V.A.
6. Autio-Harmainen, H.; Rapola, J. Renal pathology of fetuses with congenital nephrosis of the finnish type Nephron 1981 10.1159/000182343 29 158
7. Pavone, L.; Mollica, F.; Incorpora, G.; Pampiglione, G. Infantile spasm syndrome in two monozygotic twins Arch Dis Child 1980 10.1136/adc.55.11.870 55 870
8. Grunnet, M.L.; Bale, J.F. Brain abnormalities in isifants with Potter syndrome (oligohydramnios tetrad) Neurology (NY) 1981 31 15714