Evaluation Of Autosomal Recessive Polycystic Kidney Disease And Apraxias Fibrosis Kidney Diseases Polycystic Kidney Diseases Oculocerebrorenal Syndrome Polycystic Kidney, Autosomal Recessive Caroli Disease Liver Cirrhosis Coma Apnea Ataxia Muscle http://clinicaltrials.gov/ct2/show/NCT00068224
Oculocerebrorenal Syndrome - Definition Of Oculocerebrorenal syn drome (s n dr m) n. 1. A group of symptoms that collectively indicate or characterize a disease, psychological disorder, or other abnormal condition. http://www.thefreedictionary.com/oculocerebrorenal syndrome
OCRL - Wikipedia, The Free Encyclopedia Inositol polyphosphate 5phosphatase OCRL-1 (INPP5F) also known as Lowe oculocerebrorenal syndrome protein is an enzyme that in humans is encoded by the OCRL gene located on http://en.wikipedia.org/wiki/OCRL
OCRL - Oculocerebrorenal Syndrome Of Lowe Mutations linked to the disease oculocerebrorenal syndrome of Lowe led to the identification of the OCRL gene. The encoded protein is a phospatidylinositol polyphosphate 5 http://www.urogene.org/kgdb/gene/37.html
Lowe's Oculocerebrorenal Syndrome - What Does OCRL Stand For Acronym Definition; OCRL Lowe's Oculocerebrorenal Syndrome OCRL Optical Communication Research Lab (Stanford University) http://acronyms.thefreedictionary.com/Lowe's Oculocerebrorenal Syndrome
Lowe's Syndrome - Definition Of Lowe's Syndrome In The Medical Lowe's syndrome (l z) n. See oculocerebrorenal syndrome. Lowe's syndrome. A rare inherited disorder that is distinguished by congenital cataracts, glaucoma, and severe mental http://medical-dictionary.thefreedictionary.com/Lowe's syndrome
Oculocerebrorenal Dystrophy (Lowe Syndrome) EMedicine Pediatrics The diagnostic triad of the oculocerebrorenal syndrome of Lowe (OCRL), or Lowe syndrome, includes congenital cataracts, neonatal or infantile hypotonia with subsequent mental http://emedicine.medscape.com/article/946043-overview
Clinical And Laboratory Findings In The Oculocerebrorenal Syndrome Clinical and laboratory findings in the oculocerebrorenal syndrome of Lowe, with special reference to growth and renal function http://www.faqs.org/abstracts/Health/Clinical-and-laboratory-findings-in-the-ocu
AJHG - Spectrum Of Mutations In The OCRL1Gene In The Lowe Spectrum of Mutations in the OCRL1 Gene in the Lowe Oculocerebrorenal Syndrome. Ti Lin 1, Bonnie M. Orrison 1, AnnMarie Leahey 2, Sharon F. Suchy 1, David J. Bernard 1, Richard A http://www.cell.com/AJHG/abstract/S0002-9297(07)64230-X
Arquivos De Neuro-Psiquiatria - Oculocerebrorenal Syndrome Of Lowe Arquivos de NeuroPsiquiatria Print version ISSN 0004-282X Arq. Neuro-Psiquiatr. vol.67 no.2a S o Paulo June 2009 doi 10.1590/S0004-282X2009000200027 http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X20090002000
Lowe Syndrome Information Diseases Database Lowe syndrome,LoweBickel syndrome,Lowe-Terry-MacLachlan syndrome,Oculocerebral syndrome,Oculocerebrorenal syndrome, Disease Database Information http://www.diseasesdatabase.com/ddb29146.htm
Orphanet Journal Of Rare Diseases Full Text Lowe Syndrome OlivosGlander IM, Janne PA, Nussbaum RL The oculocerebrorenal syndrome gene product is a 105-kD protein localized to the Golgi complex. Am J Hum Genet 1995 , 57 817-823. http://www.ojrd.com/content/1/1/16
CIGNA - Lowe Syndrome Roschinger W, Muntau AC, Rudolph G, et al. Carrier assessment in families with Lowe oculocerebrorenal syndrome novel mutations in the OCRL1 gene and correlation of direct DNA http://www.cigna.com/healthinfo/nord109.html
Lowe Syndrome EHow.com Lowe Syndrome. Lowe syndromealso known as Lowe disease, oculocerebrorenal syndrome and oculocerebrorenal dystrophyis a rare genetic disorder that is characterized by http://www.ehow.com/facts_5510777_lowe-syndrome.html
Lowe's (Oculo-Cerebro-Renal) Syndrome Doctor Patient UK Lowe's (OculoCerebro-Renal) Syndrome - Synonyms oculocerebrorenal syndrome, OCRL, Lowe-Terrey-MacLachlan syndrome and 4,5-bisphosphate 5-phosphat http://www.patient.co.uk/doctor/Lowe-(Oculo-cerebro-renal)-Syndrome.htm
CORNEAL KELOIDS 1. Lowe syndrome (oculocerebrorenal syndrome) 2. Trauma, usually with perforation of the iris Cibis GW, et al. Corneal keloid in Lowe's syndrome. http://telemedicine.orbis.org/bins/volume_page.asp?cid=1-2897-3505-3517
Renal Glucosuria Renal Transport Abnormalities Merck Manual It also may occur with various systemic disorders, including Fanconi syndrome, cystinosis, Wilson's disease, hereditary tyrosinemia, and oculocerebrorenal syndrome (Lowe syndrome). http://www.merck.com/mmpe/sec17/ch237/ch237e.html
