Kidney disease in hypomelanosis of Ito

Nephrology Dialysis Transplantation

Volumn 16, Issue 6, 2001, Pages 1267-1269

  Coward, Richard J M ^a,c   Anthony Risdon, R ^a   Bingham, Coralie ^b   Hattersley, Andrew T ^b   Woolf, Adrian S ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY OF EXETER   (United Kingdom)

^c Departments of Obstetrics and Gynaecology   (United Kingdom)

Author keywords

Cyst; Glomerulus; Hepatocyte nuclear factor 1 ; Hypomelanosis of Ito; Kidney disease

Indexed keywords

NUCLEAR FACTOR I; NUCLEAR FACTOR I BETA; PROGESTERONE; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; CONTROLLED STUDY; DIASTOLE; DISEASE SEVERITY; FEMALE; GENE MUTATION; HUMAN; HUMAN TISSUE; HYPERTENSION; INCONTINENTIA PIGMENTI; INTRAVENOUS UROGRAPHY; KARYOTYPE 46,XX; KIDNEY BIOPSY; KIDNEY CYST; KIDNEY DISEASE; MENSTRUAL IRREGULARITY; MYOPIA; NEWBORN; PRIORITY JOURNAL; RETINA MALFORMATION; SCOLIOSIS; THORACIC SPINE; ULTRASOUND;

EID: 0034965305     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/16.6.1267     Document Type: Article

References (7)

1. Hypomelanosis of Ito: No entity, but a cutaneous sign of mosaicism
2. Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinenti Pigmenti (IP) Consortium
3. Mutations in the hepatocyte nuclear factor-1β gene are associated with familial hypoplastic glomerulocystic kidney disease
4. An unbalanced submicroscopic translocation t(8;16) (q24;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito
5. Glomerulopathy and hypomelanosis of Ito
6. Chapter 26. Developmental defects and cystic diseases of the kidney