Nephronophthisis Classification and external resources ICD-10 Q61.8 ICD-9 753.16 OMIM 256100 DiseasesDB 29224
The disorder is inherited in an autosomal recessive fashion and, although rare, is the most common genetic cause of childhood kidney failure.
Its incidence has been estimated to be 0.9 per million people in the United States, and 1 in 50.000 births in Canada.
Infantile, juvenile, and adolescent forms of nephronophthisis have been identified. Although the range of characterizations is broad, patients typically present with polyuria (production of large volume of urine), polydipsia (excessive liquid intake), and mild proteinuria (the abnormal appearance of protein in the urine), and after several months to years, end-stage kidney disease, a condition necessitating either dialysis or a kidney transplant in order to survive.
Approximately 10% of individuals with nephronophthisis also have so-called "extra-renal symptoms" which can include blindness, liver problems, severe global developmental delay or mental retardation, and neurologic involvement in which the cerebellum is affected.
Histologically, nephronophthisis is characterized by fibrosis and the formation of cysts in a specific region of the kidney. In contrast to other cystic diseases of the kidney in which the kidneys are larger than usual, in nephronophthisis the kidneys are small to normal in size.
From sequencing the DNA of individuals and families with nephronophthisis, scientists have identified thus far 8 different genes in which mutations can cause the disease. These genes are called NPHP1, NPHP2, NPHP3, NPHP4, NPHP5, NPHP6, NPHP7, and NPHP8, and the proteins for which they encode are known as the nephrocystins. Although the biological function of these proteins is not yet known, they all localize at least in part to an organelle in the cell called the primary cilia.
Relation to other rare genetic disorders
Recent findings in genetic research have suggested that a large number of genetic disorders, both genetic syndromes and genetic diseases, that were not previously identified in the medical literature as related, may be, in fact, highly related in the genetypical root cause of the widely-varying, phenotypically-observed disorders. Thus, Nephronophthisis is a ciliopathy. Other known ciliopathies include primary ciliary dyskinesia, Bardet-Biedl syndrome, polycystic kidney and liver disease, Alstrom syndrome, Meckel-Gruber syndrome and some forms of retinal degeneration.
- ^ Hurd TW, Hildebrandt F (2011). "Mechanisms of nephronophthisis and related ciliopathies". Nephron Exp. Nephrol. 118 (1): e9–e14. doi:10.1159/000320888. PMC 2992643. PMID 21071979. http://content.karger.com/produktedb/produkte.asp?typ=fulltext&file=000320888.
- ^ page 831, Chapter 35, in: Avner, Ellis D.; Harmon, William; Niaudet, Patrick; Yoshikawa, Norishige. Pediatric Nephrology (Avner, Pediatric Nephrology). Springer. ISBN 978-3-540-76327-7. (stating the incidence in the United States as 9 per 8.3 million people.
- ^ Badano, Jose L.; Norimasa Mitsuma, Phil L. Beales, Nicholas Katsanis (Sep 2006). "The Ciliopathies : An Emerging Class of Human Genetic Disorders". Annual Review of Genomics and Human Genetics 7: 125–148. doi:10.1146/annurev.genom.7.080505.115610. PMID 16722803. http://arjournals.annualreviews.org/doi/abs/10.1146/annurev.genom.7.080505.115610. Retrieved 2008-06-15.
Health science - Medicine - Cystic diseases Respiratory system Skin
stratified squamous: follicular infundibulum (Epidermoid cyst/Proliferating epidermoid cyst · Milia · Eruptive vellus hair cyst) · outer root sheath (Trichilemmal cyst/Pilar cyst/Proliferating trichilemmal cyst/Malignant trichilemmal cyst) · sebacious duct (Steatocystoma multiplex/Steatocystoma simplex) · KeratocystAdenoid cystic carcinoma · Breast cyst
Musculoskeletal system Digestive system Nervous systemCystic leukoencephalopathy Genitourinary system Other conditionsHydatid cyst · Von Hippel-Lindau syndrome · Tuberous sclerosis Congenital malformations and deformations of urinary system (Q60–Q64, 753) AbdominalKidney Pelvic Vestigial Genetic disorder, organelle: Ciliopathy Structural SignalingNephronophthisis Other/ungrouped
Wikimedia Foundation. 2010.
Look at other dictionaries:
nephronophthisis — neph·ron·oph·thi·sis (nef″ron ofґthĭ sis) [nephron + phthisis] wasting disease of the kidney substance … Medical dictionary
Nephronophthisis 1 (NPH1) — A childhood kidney disease in which there is progressive symmetrical destruction of the kidneys involving both the tubules and glomeruli, characteristically resulting in anemia, polyuria, polydipsia, isosthenuria (decreased ability to concentrate … Medical dictionary
Familial juvenile nephronophthisis (FJN) — A childhood genetic kidney disease in which there is progressive symmetrical destruction of the kidneys involving both the tubules and glomeruli, characteristically resulting in anemia, polyuria, polydipsia, isosthenuria (decreased ability to… … Medical dictionary
familial juvenile nephronophthisis — 1. a progressive hereditary disease of the kidneys characterized clinically by anemia, polyuria, and renal loss of sodium, progressing to chronic renal failure; pathological characteristics include tubular atrophy, interstitial fibrosis,… … Medical dictionary
NPHP1 — Nephronophthisis 1 (juvenile) PDB rendering based on 1s1n … Wikipedia
NPHP4 — Nephronophthisis 4 Identifiers Symbols NPHP4; FLJ46306; KIAA0673; POC10; SLSN4 External IDs … Wikipedia
NPHP3 — Nephronophthisis 3 (adolescent) Identifiers Symbols NPHP3; DKFZp667K242; DKFZp781K1312; FLJ30691; FLJ36696; KIAA2000; MGC78666; MKS7; NPH3; RHPD External IDs … Wikipedia
нефронофтиз ювенильный — (nephronophthisis juvenilis; нефрон + греч. phthisis истощение) см. Фанкони нефронофтиз … Большой медицинский словарь
Нефронофти́з юзени́льный — (nephronophthisis juvenilis; Нефрон + греч. phthisis истощение) см. Фанкони нефронофтиз … Медицинская энциклопедия
Nephronophthise — Klassifikation nach ICD 10 N11.8 Sonstige chronische tubulointerstitielle Nephritis … Deutsch Wikipedia